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Reference SNP (refSNP) Cluster Report: rs755251                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:86/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqbySubmitterwith2hitwithHapMapFreqWith1000GenomeData
Citation:PubMedLitVarNEW
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:A/G/T (FWD)
Allele Origin:
Ancestral Allele:G
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:G=0.3812/1909 (1000 Genomes)
G=0.3576/44900 (TOPMED)
HGVS Names
  • CM000677.2:g.48519823A>G
  • CM000677.2:g.48519823A>T
  • NC_000015.10:g.48519823A>G
  • NC_000015.10:g.48519823A>T
  • NC_000015.9:g.48812020A>G
  • NG_008805.2:g.130966T>A
  • NG_008805.2:g.130966T>C
  • NM_000138.4:c.1147+836T>A
  • NM_000138.4:c.1147+836T>C
Links , Linkout
SNP Details are organized in the following sections:
GeneView Map Submission Fasta Resource Diversity Validation

  Integrated Maps (Hint: click on 'Chr Pos' to see variant in the new NCBI variation viewer) back to top

  GeneView back to top

GeneView via direct blast against RefSeq sequences (used when no gene model is available): N/A


  Submitter records for this RefSNP Cluster back to top
The submission ss282245453 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs755251 during BLAST analysis for the current build.


NCBI
Assay ID
Handle|Submitter IDValidation
Status
ss to rs
Orientation
/Strand
Alleles5' Near Seq 30 bp3' Near Seq 30 bpEntry
Date
Update
Date
Build
Added
Molecule
Type
Freq
Warning
Ancestral
Allele
Success
Rate
ss109321TSC-CSHL|TSC0146875byFreqfwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag09/06/0004/07/0486Genomic95 %
ss10774969BCM_SSAHASNP|chr15.NT_010194.15_19601631fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag06/30/0310/10/03116Genomicunknown
ss16669217CSHL-HAPMAP|CSHL-HuAA-200402.chr15.NT_010194.16_19602577fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag02/17/0403/04/04120Genomicunknown
ss23431082PERLEGEN|afd2555383byFreqfwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag08/10/0409/13/04123Genomicunknown
ss43709837ABI|hCV1865677byFreqfwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag07/18/0511/03/06126Genomicunknown
ss66787514ILLUMINA|HumanHap300v1.1_rs755251fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag11/09/0611/09/06127Genomicunknown
ss67797441ILLUMINA|HumanHap550v1.1_rs755251fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag11/14/0611/14/06127Genomicunknown
ss67970734ILLUMINA|HumanHap650Yv1.0_rs755251fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag11/14/0611/15/06127Genomicunknown
ss70933148ILLUMINA|HumanHap550v3.0__rs755251rev/BC/Tcttgcaaagaacatttgctacttagcacagatttagagtcccaaatctaatcccagttca04/20/0703/31/08130Genomicunknown
ss71535237ILLUMINA|HumanHap650Yv3.0_rs755251fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag04/23/0704/23/07127Genomicunknown
ss75803133ILLUMINA|ILMN_Human_1M_rs755251fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag08/28/0708/29/07129Genomicunknown
ss79260296ILLUMINA|HumanHap300v2.0_rs755251fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag04/18/0711/18/07130Genomicunknown
ss80702112HGSV|Cor18507_SNV_20070510.chr15_46599312fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag11/26/0711/26/07130Genomicunknown
ss83551394KRIBB_YJKIM|KHS487908fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag12/04/0712/05/07130Genomicunknown
ss84338197HGSV|Cor19240_SNV_20070510.chr15_46599312fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag11/30/0712/07/07130Genomicunknown
ss96809279HUMANGENOME_JCVI|1103645604954fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag03/27/0803/27/08130Genomicunknown
ss1141383331000GENOMES|NA19240_2008_12_16_2834790_chr15_46599312fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag12/18/0812/18/08130Genomicunknown
ss118217248ILLUMINA-UK|NA18507_000032587_NCBI36.1_chr15_46599312fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag01/20/0901/21/09130Genomic99 %
ss122776359ILLUMINA|HumanCNV370v1_C_rs755251fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag04/14/0904/15/09131Genomicunknown
ss136910899ENSEMBL|ENSSNP1104060byFreqfwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag12/08/0803/07/10131Genomicunknown
ss154429612ILLUMINA|Human610_Quadv1_B_rs755251-127_B_R_1501867844rev/BC/Tcttgcaaagaacatttgctacttagcacagatttagagtcccaaatctaatcccagttca06/18/0906/20/09131Genomicunknown
ss156510176GMI|GMI_SNP_132065428fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag06/24/0906/25/09131Genomicunknown
ss159604720ILLUMINA|Human660W-Quad_v1_A_rs755251-128_B_R_1501867844rev/BC/Tcttgcaaagaacatttgctacttagcacagatttagagtcccaaatctaatcccagttca07/06/0907/07/09131Genomicunknown
ss160887639ILLUMINA|HumanOmni1-Quad_v1-0_B_rs755251-128_B_R_1501867844rev/BC/Tcttgcaaagaacatttgctacttagcacagatttagagtcccaaatctaatcccagttca08/04/0910/04/09131Genomicunknown
ss169380380COMPLETE_GENOMICS|NA19240_36_chr15_46599312fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag10/01/0910/01/09132Genomicunknown
ss171059440COMPLETE_GENOMICS|NA20431_36_chr15_46599312fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag10/01/0910/01/09132Genomicunknown
ss172304961ILLUMINA|HumanCNV370-Quadv3_C_rs755251-127_B_R_1501867844rev/BC/Tcttgcaaagaacatttgctacttagcacagatttagagtcccaaatctaatcccagttca10/01/0910/04/09132Genomicunknown
ss174413490ILLUMINA|Human1M-Duov3_B_rs755251-127_B_R_1501867844rev/BC/Tcttgcaaagaacatttgctacttagcacagatttagagtcccaaatctaatcccagttca10/01/0910/04/09132Genomicunknown
ss200813902BUSHMAN|BUSHMAN-chr15-46599311fwd/TA/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag02/16/1003/07/10132Genomicunknown
ss2268802821000GENOMES|pilot_1_YRI_8689965_chr15_46599312fwd/A/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag04/22/1004/22/10132Genomicunknown
ss2367690841000GENOMES|pilot_1_CEU_6373713_chr15_46599312fwd/A/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag05/01/1005/01/10132Genomicunknown
ss2431575701000GENOMES|pilot_1_CHB+JPT_5042647_chr15_46599312fwd/A/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag05/01/1005/01/10132Genomicunknown
ss282245453GMI|GMI_AK_SNP_6565852fwd/A/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag12/16/1012/16/10137Genomicunknown
ss291715441PJP|SNP_1221799_chr15_46599312fwd/A/Gtgaactgggattagatttgggactctaaatctgtgctaagtagcaaatgttctttgcaag01/21/1101/21/11134Genomicunknown
ss481591870ILLUMINA|HumanOmni2.5-4v1_B_rs755251-128_B_R_1630037782fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt01/30/1210/28/16137Genomicunknown
ss481621849ILLUMINA|HumanOmniExpress-12v1_C_rs755251-131_B_R_1857302562fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt01/30/1210/27/16137Genomicunknown
ss482591716ILLUMINA|HumanOmni1-Quad_v1-0_C_rs755251-131_B_R_1865230045fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt01/30/1208/28/15146Genomicunknown
ss485590875ILLUMINA|HumanOmni2.5-4v1_D_rs755251-131_B_R_1857302562fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt01/30/1210/27/16137Genomicunknown
ss537481455ILLUMINA|HumanOmni5-4v1_B_rs755251-131_B_R_1894040979fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt06/22/1208/29/15146Genomicunknown
ss564466957TISHKOFF|snp_chr15_48812020fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt11/22/1211/23/12138Genomicunknown
ss660187184SSMP|15_48812020fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt12/14/1202/13/15138Genomicunknown
ss778605978ILLUMINA|HumanOmni25Exome-8v1_A_rs755251-131_B_R_1865230045fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt05/30/1307/10/15146Genomicunknown
ss783241036ILLUMINA|HumanOmni2.5-4v1_H_rs755251-131_B_R_1857302562fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt05/30/1307/29/15146Genomicunknown
ss784194856ILLUMINA|HumanOmniExpressExome-8v1_A_rs755251-131_B_R_1894040979fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt05/31/1306/18/15146Genomicunknown
ss825590814ILLUMINA|HumanCNV370v1_C_rs755251-126_B_R_IFB1136776939:0fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt06/24/1311/21/14147Genomicunknown
ss832501612ILLUMINA|HumanOmniExpress-12v1_H_rs755251-131_B_R_1857302562fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt09/17/1306/18/15146Genomicunknown
ss834063329ILLUMINA|HumanOmni2.5-8v1_A_rs755251-131_B_R_1865230045fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt09/18/1307/29/15146Genomicunknown
ss991761827EVA-GONL|EVA-GONL_rs755251fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt04/23/1404/30/14142Genomicunknown
ss1080106063JMKIDD_LAB|HGDP_WGS_chr15_48812020fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt07/10/1407/12/14142Genomicunknown
ss13533686681000GENOMES|PHASE3_V1_66697110fwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt08/16/1408/16/14142Genomicunknown
ss1427618035DDI|DDI_rs755251fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt11/04/1411/04/14144Genomicunknown
ss1577599407EVA_GENOME_DK|EVA_GENOME_DK_snv_rs755251fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt02/19/1502/19/15144Genomicunknown
ss1632945706EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_15_48812020_36879004fwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt03/04/1503/04/15144Genomicunknown
ss1675939739EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_15_48812020_36879004fwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt03/04/1503/04/15144Genomicunknown
ss1695778057EVA_DECODE|EVA_DECODE_15_46599312_192633_rs755251fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt03/02/1503/04/15144Genomicunknown
ss1713487971EVA_SVP|EVA_SVP_1182338fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt03/12/1503/12/15144Genomicunknown
ss1752162032ILLUMINA|OmniExpressExome-8v1-1_B_rs755251-131_B_R_1894040979fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt05/27/1506/09/15146Genomicunknown
ss1808192921HAMMER_LAB|Hsieh_7217894fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt07/15/1507/16/15146Genomicunknown
ss1935165610WEILL_CORNELL_DGM|SNV:chr15:48812020fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt10/16/1510/18/15147Genomicunknown
ss1968100508GENOMED|rs755251fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt02/16/1602/16/16147Genomicunknown
ss2028361941JJLAB|SNP8864496fwd/TA/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt08/29/1608/31/16149Genomicunknown
ss2156763015USC_VALOUEV|NC_000015.9:g.48812020A>Gfwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt11/17/1611/17/16150Genomicunknown
ss2206577798HUMAN_LONGEVITY|HLI-15-48519823-A-Gfwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt11/18/1611/18/16150Genomicunknown
ss2371252748TOPMED|15_48812020_A/Gfwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt11/19/1611/19/16150Genomicunknown
ss2628674913SYSTEMSBIOZJU|SYSTEMSBIOZJU_SNV5663472fwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt01/06/1701/06/17151Genomicunknown
ss2633225836ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_rs755251-131_B_R_189404097fwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt02/02/1702/02/17151Genomicunknown
ss2701231990GRF|rs755251fwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt02/13/1702/13/17151Genomicunknown
ss2934630146GNOMAD|rs755251fwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt05/23/1705/23/17151Genomicunknown
ss3013243612SWEGEN|NC_000015.9:g.48812020A>Gfwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt05/30/1705/30/17151Genomicunknown
ss3028004015BIOINF_KMB_FNS_UNIBA|15.48519823A>Gfwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt07/05/1707/05/17151Genomicunknown
ss3227008840TOPMED|TOPMed_freeze_5?chr15:48,519,823-01fwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt10/01/1710/01/17151Genomicunknown
ss3227008841TOPMED|TOPMed_freeze_5?chr15:48,519,823-02fwd/A/Ttgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt10/01/1710/01/17151Genomicunknown
ss3351104096CSHL|rs755251fwd/A/Gtgggattagatttgggactctaaatctgtgctaagtagcaaatgttcttt10/02/1710/02/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs755251|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='A/G/T'|mol=Genomic|build=151
 GGAAAGATGT TGCCTAATAA GTTGCTCTCT GTATTTGAAT GCCTCCTATA AGCAAGATTT
 TGCTAAATAC TATGGAAGTG TAAAAAGCAT GAGAAATATG AGACTACAAT AATGAATGAG
 ATTTCCTAAT GAGATTGATC AACCAGTAAA AGAGCAAGAT GTGAACACAC ATATGGCACT
 CATGCCATAG TGATAGTACC AGCCAGAACC ACAGGAGCAC AAGGAAGAAG GGAGCACTTC
 CAGCTGCAGG TACCTCGGGA TATTCATGGA TTAGGTCATG TTTGAGCAGA TCCTTAACAA
 GAAAAGAGGA TATATAACAG GCAAGGATGG CAGGAGTAGG GAGAAAGAGC CTGAACTGGC
 AAGAAGTTTT AGAAAAAAAA GCCAACTTGA ATTCAGAAAT GCTCGGATTG GGTGCAATGA
 AAACTCAATC ATATAATTTA AACTACTATA AAGAACAAGA ATTAAAAAGA TGAACTGGGA
 TTAGATTTGG GACTCTAAAT
 D
 CTGTGCTAAG TAGCAAATGT TCTTTGCAAG AAATGGAGTG AATTGGCCAC TAAATATTGC
 CTGAGTTCAT CCTGGGGAAA TATTTTTGGA CATCTTTCTC GACTAACGAA AGTGTGCTGT
 ATTTATGTAT TTGTTTAGTT ATGTATTTTT AAACTAATGA ATAAAAATTG TATGCATTCA
 TTGTGTACAA CATGGTGTTT TGAAATAGGC TCAATTAGTC AAAAGGTGTC TCCTTTTTCT
 CCCCTAGACA CAATTTTTTA AACTGAACTT CACTGACTCA TACTTTGGGA AAGGTACATG
 GCAATGGTGG ATTTCAGAGA CTAGTTAGGA GACTACTGGA ACAGTCCAGA CTAGAGAAAA
 TACGCTTCTA ATAGAAACAA AAAAATGGAC AGATAAAAGA GATACTGTGA AGGAAAAAAA
 AAACAAGCAG GACTTAGCAG GAAGGAAAGA GTCCAATGTT AGGAAAAAGG AAATGTGTCT
 CCTGAACAAC TTACCTGAAA

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_010194 ABBA01039137
dbSNP Blast Analysis

  Population Diversity (Alleles in RefSNP orientation) . See additional population frequency from 1000Genome [here] back to top

Sample AscertainmentGenotype DetailAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/G
G/G
HWPA
G
ss109321HapMap-CEUEuropean 226IG0.584070800.345132740.070796460.527089000.756637160.24336283
HapMap-HCBAsian 86IG0.465116290.511627910.023255810.099721000.720930220.27906978
HapMap-JPTAsian 172IG0.302325580.430232550.267441870.200325000.517441870.48255813
HapMap-YRISub-Saharan African 226IG0.113475170.546099310.340425520.099721000.380530980.61946905
HAPMAP-ASW 98IG0.169811320.377358500.452830200.200325000.367346940.63265306
HAPMAP-CHBAsian 82IG0.243902440.634146330.121951220.099721000.560975610.43902439
HAPMAP-CHD 170IG0.388235300.470588240.141176481.000000000.623529430.37647060
HAPMAP-GIH 174IG0.609195410.310344820.080459770.200325000.764367820.23563218
HAPMAP-LWK 180IG0.155555560.444444450.400000010.654721000.377777790.62222224
HAPMAP-MEX 100IG0.610389590.311688300.077922080.150222000.790000020.20999999
HAPMAP-MKK 286IG0.286713270.426573430.286713270.099721000.500000000.50000000
HAPMAP-TSI 176IG0.579545440.363636370.056818181.000000000.761363630.23863636
ENSEMBL_Watson 2IG1.00000000 1.00000000
ss118217248YRI 2IG 1.00000000 1.00000000
ss1353368668EAS 1008AF 0.647800030.35220000
EUR 1006AF 0.743499990.25650001
AFR 1322AF 0.344899980.65509999
AMR 694AF 0.733400050.26660001
SAS 978AF 0.749499980.25049999
ss136910899ENSEMBL_Venter 2IG 1.00000000 0.500000000.50000000
ENSEMBL_celera 4IG0.50000000 0.50000000 0.500000000.50000000
ss169380380YRISub-Saharan African 2IG 1.00000000 1.00000000
ss171059440PGP 2IG 1.00000000 0.500000000.50000000
ss200813902BUSHMAN_POP2 2IG 1.00000000 0.500000000.50000000
ss226880282pilot_1_YRI_low_coverage_panel 118AF 0.381355940.61864406
ss23431082AFD_EUR_PANELEuropean 48IG0.583333310.291666660.125000000.200325000.729166690.27083334
AFD_AFR_PANELAfrican American 44IG0.272727280.454545470.272727280.751830000.500000000.50000000
AFD_CHN_PANELAsian 48IG0.416666660.458333340.125000001.000000000.645833310.35416666
ss236769084pilot_1_CEU_low_coverage_panel 120AF 0.741666670.25833333
ss243157570pilot_1_CHB+JPT_low_coverage_panel 120AF 0.616666670.38333333
ss43709837AoD_Caucasian 92AF 0.829999980.17000000
ss96809279J. Craig Venter 2IG 1.00000000 0.500000000.50000000

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
Additional Freq. Data
0.472+/-0.1150000ALFRED: The Allele Frequency Database

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqbySubmitterwith2hitwithHapMapFreqWith1000GenomeData
Validated by: PERLEGEN
DoubleHit found by:  BCM_SSAHASNPNCBI
UNKNOWNUNKNOWNUNKNOWN

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