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Reference SNP (refSNP) Cluster Report: rs1036477                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:86/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqbySubmitterwith2hitWith1000GenomeData
Citation:PubMedLitVarNEW
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:A/G (FWD)
Allele Origin:
Ancestral Allele:G
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:G=0.2943/1474 (1000 Genomes)
G=0.2590/32517 (TOPMED)
HGVS Names
  • CM000677.2:g.48622729A>G
  • NC_000015.10:g.48622729A>G
  • NC_000015.9:g.48914926A>G
  • NG_008805.2:g.28060T>C
  • NM_000138.4:c.165-9637T>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 ss1502534 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs1036477 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
ss1502534TSC-CSHL|TSC0341283byFreqfwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc09/07/0004/07/0486Genomic95 %
ss3458136SC_JCM|AC084757.2_22482fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc09/24/0110/10/03100Genomicunknown
ss10764280BCM_SSAHASNP|chr15.NT_010194.15_19704537fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc06/30/0310/10/03116Genomicunknown
ss23646582PERLEGEN|afd1057529byFreqfwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc08/10/0409/13/04123Genomicunknown
ss66535579AFFY|SNP_A-4240107byFreqfwd/TA/Ggcctaatctacctgtcactcttatctttacct10/29/0608/14/07127Genomicunknown
ss66569696ILLUMINA|HumanHap300v1.1_rs1036477fwd/BA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc11/09/0611/09/06127Genomicunknown
ss69175629PERLEGEN|PGP01057529byFreqfwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc01/30/0708/14/07127Genomicunknown
ss70364671ILLUMINA|HumanHap300v2.0_rs1036477fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc04/18/0711/17/07127Genomicunknown
ss70476981ILLUMINA|HumanHap550v3.0__rs1036477rev/BC/Tgaagttgaaggtataggtaaagataagagtgacaggtagattaggcctacctggtagata04/20/0703/29/08130Genomicunknown
ss70999994ILLUMINA|HumanHap650Yv3.0_rs1036477fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc04/23/0704/23/07127Genomicunknown
ss74941023ILLUMINA|ILMN_Human_1M_rs1036477fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc08/28/0708/29/07129Genomicunknown
ss76357997AFFY|AFFY_6_1M_SNP_A-4240107byFreqfwd/TA/Ggcctaatctacctgtcactcttatctttacct08/28/0703/07/10129Genomicunknown
ss78683002HGSV|Cor18507_SNV_20070510.chr15_46702218fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc10/19/0710/20/07129Genomicunknown
ss81452320KRIBB_YJKIM|KHS78505fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc11/30/0711/30/07130Genomicunknown
ss84569603HGSV|Cor19129_SNV_20070510.chr15_46702218fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc12/06/0712/07/07130Genomicunknown
ss1141390321000GENOMES|NA19240_2008_12_16_2834878_chr15_46702218fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc12/18/0812/18/08130Genomicunknown
ss118217543ILLUMINA-UK|NA18507_000032727_NCBI36.1_chr15_46702218fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc01/20/0901/21/09130Genomic99 %
ss121299775ILLUMINA|HumanCNV370v1_C_rs1036477fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc04/14/0904/14/09131Genomicunknown
ss152715750ILLUMINA|Human610_Quadv1_B_rs1036477-128_B_R_1501597064rev/BC/Tgaagttgaaggtataggtaaagataagagtgacaggtagattaggcctacctggtagata06/18/0906/19/09131Genomicunknown
ss159121573ILLUMINA|Human660W-Quad_v1_A_rs1036477-128_B_R_1501597064rev/BC/Tgaagttgaaggtataggtaaagataagagtgacaggtagattaggcctacctggtagata07/06/0907/06/09131Genomicunknown
ss159888420ILLUMINA|HumanOmni1-Quad_v1-0_B_rs1036477-128_B_R_1501597064rev/BC/Tgaagttgaaggtataggtaaagataagagtgacaggtagattaggcctacctggtagata08/04/0910/01/09131Genomicunknown
ss169366840ILLUMINA|HumanCNV370-Quadv3_C_rs1036477-128_B_R_1501597064rev/BC/Tgaagttgaaggtataggtaaagataagagtgacaggtagattaggcctacctggtagata10/01/0910/02/09132Genomicunknown
ss169382062COMPLETE_GENOMICS|NA19240_36_chr15_46702218fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc10/01/0910/01/09132Genomicunknown
ss170010358ILLUMINA|Human1M-Duov3_B_rs1036477-128_B_R_1501597064rev/BC/Tgaagttgaaggtataggtaaagataagagtgacaggtagattaggcctacctggtagata10/01/0910/01/09132Genomicunknown
ss171059997COMPLETE_GENOMICS|NA20431_36_chr15_46702218fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc10/01/0910/01/09132Genomicunknown
ss173373891AFFY|GenomeWideSNP_5_SNP_A-4240107fwd/TA/Ggcctaatctacctgtcactcttatctttacct10/01/0910/03/09132Genomicunknown
ss200814408BUSHMAN|BUSHMAN-chr15-46702217fwd/TA/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc02/16/1003/07/10132Genomicunknown
ss2268805961000GENOMES|pilot_1_YRI_8690279_chr15_46702218fwd/A/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc04/22/1004/22/10132Genomicunknown
ss2367692491000GENOMES|pilot_1_CEU_6373878_chr15_46702218fwd/A/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc05/01/1005/01/10132Genomicunknown
ss2431577441000GENOMES|pilot_1_CHB+JPT_5042821_chr15_46702218fwd/A/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc05/01/1005/01/10132Genomicunknown
ss244268654ILLUMINA|CVDSNP55v1_A_rs1036477rev/BC/Tgaagttgaaggtataggtaaagataagagtgacaggtagattaggcctacctggtagata06/10/1006/10/10132Genomicunknown
ss282245607GMI|GMI_AK_SNP_6566006fwd/A/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc12/16/1012/16/10137Genomicunknown
ss291715523PJP|SNP_1221881_chr15_46702218fwd/A/Gtatctaccaggtaggcctaatctacctgtcactcttatctttacctataccttcaacttc01/21/1101/21/11134Genomicunknown
ss479253805ILLUMINA|HumanOmni2.5-4v1_B_rs1036477-128_B_R_1630037792fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca01/30/1210/28/16137Genomicunknown
ss479256682ILLUMINA|HumanOmniExpress-12v1_C_rs1036477-131_B_R_1857073363fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca01/30/1210/27/16137Genomicunknown
ss479619556ILLUMINA|HumanOmni1-Quad_v1-0_C_rs1036477-131_B_R_1865736455fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca01/30/1208/28/15146Genomicunknown
ss484427606ILLUMINA|HumanOmni2.5-4v1_D_rs1036477-131_B_R_1857073363fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca01/30/1210/27/16137Genomicunknown
ss536600675ILLUMINA|HumanOmni5-4v1_B_rs1036477-131_B_R_1891268925fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca06/22/1208/29/15146Genomicunknown
ss564467345TISHKOFF|snp_chr15_48914926fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca11/22/1211/23/12138Genomicunknown
ss660187554SSMP|15_48914926fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca12/14/1202/13/15138Genomicunknown
ss778730076ILLUMINA|HumanOmni25Exome-8v1_A_rs1036477-131_B_R_1865736455fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca05/30/1307/10/15146Genomicunknown
ss782660261ILLUMINA|HumanOmni2.5-4v1_H_rs1036477-131_B_R_1857073363fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca05/30/1307/29/15146Genomicunknown
ss783629312ILLUMINA|HumanOmniExpressExome-8v1_A_rs1036477-131_B_R_1891268925fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca05/31/1306/18/15146Genomicunknown
ss825334402ILLUMINA|HumanCNV370v1_C_rs1036477-123_B_R_IFB1135079953:0fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca06/24/1311/21/14144Genomicunknown
ss831910758ILLUMINA|HumanOmniExpress-12v1_H_rs1036477-131_B_R_1857073363fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca09/17/1306/18/15146Genomicunknown
ss834189554ILLUMINA|HumanOmni2.5-8v1_A_rs1036477-131_B_R_1865736455fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca09/18/1307/29/15146Genomicunknown
ss991762379EVA-GONL|EVA-GONL_rs1036477fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca04/23/1404/30/14142Genomicunknown
ss1080106516JMKIDD_LAB|HGDP_WGS_chr15_48914926fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca07/10/1407/12/14142Genomicunknown
ss13533712341000GENOMES|PHASE3_V1_66699767fwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca08/16/1408/16/14142Genomicunknown
ss1427618120DDI|DDI_rs1036477fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca11/04/1411/04/14144Genomicunknown
ss1577599590EVA_GENOME_DK|EVA_GENOME_DK_snv_rs1036477fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca02/19/1502/19/15144Genomicunknown
ss1632947106EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_15_48914926_36880522fwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca03/04/1503/04/15144Genomicunknown
ss1675941139EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_15_48914926_36880522fwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca03/04/1503/04/15144Genomicunknown
ss1695778635EVA_DECODE|EVA_DECODE_15_46702218_193211_rs1036477fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca03/02/1503/04/15144Genomicunknown
ss1713488016EVA_SVP|EVA_SVP_1182383fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca03/12/1503/12/15144Genomicunknown
ss1752162054ILLUMINA|OmniExpressExome-8v1-1_B_rs1036477-131_B_R_1891268925fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca05/27/1506/09/15146Genomicunknown
ss1808193116HAMMER_LAB|Hsieh_7218089fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca07/15/1507/16/15146Genomicunknown
ss1935166206WEILL_CORNELL_DGM|SNV:chr15:48914926fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca10/16/1510/18/15147Genomicunknown
ss2028362156JJLAB|SNP8864711fwd/TA/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca08/29/1608/31/16149Genomicunknown
ss2156763297USC_VALOUEV|NC_000015.9:g.48914926A>Gfwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca11/17/1611/17/16150Genomicunknown
ss2206583432HUMAN_LONGEVITY|HLI-15-48622729-A-Gfwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca11/18/1611/18/16150Genomicunknown
ss2371258424TOPMED|15_48914926_A/Gfwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca11/19/1611/19/16150Genomicunknown
ss2628675032SYSTEMSBIOZJU|SYSTEMSBIOZJU_SNV5663626fwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca01/06/1701/06/17151Genomicunknown
ss2633225890ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_rs1036477-131_B_R_18912689fwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca02/02/1702/02/17151Genomicunknown
ss2701232318GRF|rs1036477fwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca02/13/1702/13/17151Genomicunknown
ss2934637570GNOMAD|rs1036477fwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca05/23/1705/23/17151Genomicunknown
ss3013244526SWEGEN|NC_000015.9:g.48914926A>Gfwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca05/30/1705/30/17151Genomicunknown
ss3021631089ILLUMINA|MEGA_Consortium_v2_15070954_A2_rs1036477-138_B_R_2258092171fwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca06/28/1706/28/17151Genomicunknown
ss3028004129BIOINF_KMB_FNS_UNIBA|15.48622729A>Gfwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca07/05/1707/05/17151Genomicunknown
ss3227026125TOPMED|TOPMed_freeze_5?chr15:48,622,729fwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca10/01/1710/01/17151Genomicunknown
ss3351104265CSHL|rs1036477fwd/A/Gaccaggtaggcctaatctacctgtcactcttatctttacctataccttca10/02/1710/02/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs1036477|allelePos=355|totalLen=1207|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=151
 GGTAAGCTCA GAAGAGGACT ATCTGAGCTA TGACTTGATG TTTCCCGGTT GCTAAGGGGA
 GTCACTAGTT TTATTTCATC CCACTGATGA AATTCCCCTT AAATTCTCCA ACTCCATTAG
 CAAATCCCTT GTCCAAATCC TGGTGATTTC ATTGTTGGAC CAATATCATG TTCTTTTTTC
 CTGGCTTCCT AGTTTCTCTC TACCCCATTA GGACAATATG GGTAAGTATC TTTTCATATT
 CACCGTGCTT ATTTCTATTC CCCTACAGCC CAAAGATGGA CCTTCACTCT CTATAATGTT
 AAACATCTCA TTATTAGGTT CAGATATCTA CCAGGTAGGC CTAATCTACC TGTC
 R
 ACTCTTATCT TTACCTATAC CTTCAACTTC CACCCTCCTA CTCAGCTCCT CTTCTTCACC
 GTCTCAGCCC TCACTCATGC ACGCACTGCT ATCTCTGACA CACACTAAAA CCAGACACTT
 CCTCCATTTT TATATCAGCT CTTCCATCTT TCCATTTCAA TATGTAGTTC CATCTCCCTT
 AGTGTTCCCT GATGAATCCA TCCATCTTTC ACACTACAAA CACAATTCCA GACATATCTT
 CAAAAACCTA CATAGGCTAT ACTGTAGTTA TATATTTAAA ACAATTATAT GTCTAGATCT
 CATCCCTGAA GCCCAACCCA CCACCCCCTT TACTCCCAGA GTAATAAATT GTTCTTCAGG
 CACAGAAACA ATGTCTATTA TGCCTAGACT ATCCTGGAGT CTATTTAGAA GCACACAAGA
 TAATATTGAC TAAAGGCAAT AGTGAGTACG AAGTACAATT AGCAAAGATT AATATCATCT
 CCTCAGTGCC AAAAGTAAGC CAGATGGAAT ATGCCACCGA CATTAAAATC TGTGCGATAG
 AATTATTTCT TATAAATTTA TCTATTTAAA AGAAGACTAT TTAACACGTC TTTGAAAGGC
 TACATAGGCA GTTAAACAGA AATGTATGGT GGTTTTGTGC CTTGATTATT TCACTGACAT
 GCCTGTCATT AACTTATTCT GATCAGTGAA GTTACCCATG TTTATAACTC AGAAATCAAT
 ATTTTCCTTT GAGAAAATAC AAAATCAATG TAGACAAATA ACACACATAT GTAAACATTT
 GATTCTATTT ATTTCTTTGG CAAAAGAAGA AAAAAAATCC CACAAGCAAC TAAGTGAAGG
 TTTTCAGCTC AC

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_010194 AC012290 AC022467 AC027140 AC027140.2 AC027545 AC027545.2
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
ss118217543YRI 2IG 1.00000000 0.500000000.50000000
ss1353371234EAS 1008AF 0.730200050.26980001
EUR 1006AF 0.882700030.11730000
AFR 1322AF 0.387999980.61200005
AMR 694AF 0.847299990.15270001
SAS 978AF 0.827200000.17280000
ss1502534HapMap-CEUEuropean 226IG0.814159270.168141590.017699110.402784000.898230080.10176991
HapMap-HCBAsian 86IG0.581395330.325581400.093023260.342782000.744186040.25581396
HapMap-JPTAsian 172IG0.337209310.476744170.186046511.000000000.575581370.42441860
HapMap-YRISub-Saharan African 226IG0.115044250.548672560.336283180.150222000.389380540.61061949
HAPMAP-ASW 98IG0.265306120.387755100.346938790.150222000.459183660.54081631
HAPMAP-CHBAsian 82IG0.463414640.439024390.097560971.000000000.682926830.31707317
HAPMAP-CHD 168IG0.559523820.392857130.047619050.583882000.755952360.24404761
HAPMAP-GIH 174IG0.678160910.298850570.022988510.751830000.827586230.17241380
HAPMAP-LWK 178IG0.123595510.516853930.359550570.402784000.382022470.61797750
HAPMAP-MEX 100IG0.839999970.140000000.020000000.317310000.910000030.09000000
HAPMAP-MKK 286IG0.286713270.559440550.153846160.099721000.566433550.43356642
HAPMAP-TSI 176IG0.704545440.272727280.022727271.000000000.840909060.15909091
ENSEMBL_Watson 2IG1.00000000 1.00000000
ENSEMBL_Venter 2IG1.00000000 1.00000000
ss169382062YRISub-Saharan African 2IG 1.00000000 1.00000000
ss171059997PGP 2IG 1.00000000 0.500000000.50000000
ss226880596pilot_1_YRI_low_coverage_panel 118AF 0.389830500.61016947
ss23646582AFD_EUR_PANELEuropean 48IG0.791666690.20833333 1.000000000.895833310.10416666
AFD_AFR_PANELAfrican American 46IG0.217391300.608695630.173913050.294266000.521739130.47826087
AFD_CHN_PANELAsian 48IG0.583333310.333333340.083333340.654721000.750000000.25000000
ss236769249pilot_1_CEU_low_coverage_panel 120AF 0.899999980.10000000
ss243157744pilot_1_CHB+JPT_low_coverage_panel 120AF 0.616666670.38333333
ss66535579HapMap-CEUEuropean 118IG0.847457650.135593220.016949150.342782000.915254240.08474576
HapMap-HCBAsian 90IG0.577777800.333333340.088888890.438578000.744444430.25555557
HapMap-JPTAsian 90IG0.288888900.466666670.244444440.751830000.522222220.47777778
HapMap-YRISub-Saharan African 120IG0.133333340.600000020.266666680.099721000.433333340.56666666
ss69175629HapMap-CEUEuropean 120IG0.850000020.133333340.016666670.342782000.916666690.08333334
HapMap-HCBAsian 90IG0.577777800.333333340.088888890.438578000.744444430.25555557
HapMap-JPTAsian 90IG0.288888900.466666670.244444440.751830000.522222220.47777778
HapMap-YRISub-Saharan African 120IG0.133333340.600000020.266666680.099721000.433333340.56666666
ss76357997ICMHP 8IG0.75000000 0.25000000 0.750000000.25000000

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
Additional Freq. Data
0.415+/-0.1870000ALFRED: 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
byClusterbyFreqbySubmitterwith2hitWith1000GenomeData
Validated by: PERLEGEN
DoubleHit found by:  BCM_SSAHASNPNCBI
UNKNOWNUNKNOWNUNKNOWN

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