Meta tags:
description=dbSNP is a public-domain archive for human single nucleotide variations, microsatellites, and small-scale insertions and deletions along with publication, population frequency, molecular consequence, and genomic and RefSeq mapping information for both common variations and clinical mutations.;

Headings (most frequently used words):

dbsnp, the, with, more, search, to, is, from, subjects, project, than, below, goal, provide, allele, frequency, video, introduction, view, million, information, dbgap, regular, or, variation, updates, visit, page, for, databases, here, youtube, 200k, started, submission, access, data, alfa, release, over, 900m, variants, now, announcements, available, august, 2023, how, additional, terms, are, getting, news, and, account,

Text of the page (most frequently used words):
and (12), the (12), #dbsnp (9), #search (7), #ncbi (7), #frequency (6), #gene (5), variation (4), #with (4), you (4), #single (4), information (4), #protein (4), for (4), clinical (4), more (3), all (3), government (3), allele (3), how (3), account (3), site (3), dbgap (3), pubchem (3), gov (3), significance (3), snp (3), official (3), web (3), variations (3), nlm (3), clinvar (2), help (2), provide (2), submission (2), from (2), range (2), #database (2), gtr (2), youtube (2), project (2), log (2), pathogenic (2), nucleotide (2), policies (2), homepage (2), updates (2), genomic (2), subjects (2), position (2), main (2), that (2), facebook (2), dbvar (2), page (2), databases (2), hhs (2), github (2), federal (2), population (2), insights (2), 328 (2), alfa (2), access (2), geo (2), are (2), twitter (2), 00000 (2), website (2), here (2), family, 20th, clusters, human, anniversary, started, contains, models, bioassay, compound, getting, small, substance, term, molecular, consequence, refseq, publication, along, mapping, both, common, mutations, advanced, pmc, microsatellites, toolkitbookgh, toolkitall, toolkit, deletions, insertions, taxonomy, scale, structure, sra, pubmed, popset, usa, omim, sensitive, any, encrypted, transmitted, securely, https, secure, websites, often, end, mil, before, sharing, make, ensures, sure, means, know, united, states, requires, javascript, function, warning, connecting, info, catalog, biocollections, mesh, medgen, identical, groups, profiles, datasets, genome, conserved, domains, books, biosample, bioproject, assembly, show, short, genetic, navigation, overview, myncbi, keys, out, settings, publications, dashboard, logged, username, close, content, release, required, news, announcements, 0010, 0100, global_maf, global, study, wide, minor, gmaf, note, zero, rss, padding, shown, example, 001, likely, chromosome, 1500000, 3000000, base, location, feed, list, see, pike, nih, careers, accessibility, vulnerability, disclosure, foia, national, library, medicine, 8600, rockville, bethesda, email, 20894, connect, blog, linkedin, follow, viewer, spdi, service, accessing, minute, webinar, grch38, using, reference, eutils, 900m, variants, 200k, now, august, 2023, available, tutorials, ftp, download, services, api, below, data, hold, until, published, hup, submit, entrez, may, 2020, factsheet, about, over, video, grch37, coordinates, guide, announcement, symbol, 4023, gene_id, pten, name, multiple, 226, 200, refsnp, then, introduction, use, filters, results, additional, terms, goal, than, million, regular, visit, view, home,

Text of the page (random words):
home snp ncbi warning the ncbi web site requires javascript to function more an official website of the united states government here s how you know the gov means it s official federal government websites often end in gov or mil before sharing sensitive information make sure you re on a federal government site the site is secure the https ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely log in show account info close account logged in as username dashboard publications account settings log out access keys ncbi homepage myncbi homepage main content main navigation dbsnp database of short genetic variations search database all databases assembly biocollections bioproject biosample books clinvar conserved domains dbgap dbvar gene genome geo datasets geo profiles gtr identical protein groups medgen mesh nlm catalog nucleotide omim pmc popset protein protein clusters protein family models pubchem bioassay pubchem compound pubchem substance pubmed snp sra structure taxonomy toolkit toolkitall toolkitbookgh search term search advanced help dbsnp dbsnp contains human single nucleotide variations microsatellites and small scale insertions and deletions along with publication population frequency molecular consequence and genomic and refseq mapping information for both common variations and clinical mutations getting started dbsnp 20th anniversary overview of dbsnp about reference snp rs factsheet entrez updates may 26 2020 submission how to submit hold until published hup policies submission search access data web search eutils api variation services ftp download tutorials on github alfa project release 3 with over 900m variants from 200k subjects is now available august 3 2023 the goal is to provide allele frequency from more than 1 million dbgap subjects with regular updates visit the project page for more information or view the introduction video below how to search dbsnp additional search terms are here all of dbsnp then use filters on results page all sb dbsnp refsnp id single 328 multiple 328 226 200 gene gene symbol pten gene name or gene id 4023 gene_id genomic location of a single position or range on grch38 see the announcement and the guide for using grch37 coordinates 6 chromosome and 1500000 3000000 base position clinical significance pathogenic clinical significance or likely pathogenic clinical significance global or study wide minor allele frequency gmaf of a single frequency or range note the required zero padding frequency as shown in example for 0 001 and 0 01 00000 0010 00000 0100 global_maf dbsnp news and announcements ncbi insights rss feed email list youtube ncbi minute alfa webinar accessing population allele frequency spdi and variation service variation viewer variation databases dbvar dbgap clinvar gtr follow ncbi twitter facebook linkedin github ncbi insights blog connect with nlm twitter facebook youtube national library of medicine 8600 rockville pike bethesda md 20894 web policies foia hhs vulnerability disclosure help accessibility careers nlm nih hhs usa gov