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Reference SNP (refSNP) Cluster Report: rs5979785                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:114/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqwith2hitwithHapMapFreqWith1000GenomeData
Citation:PubMedLitVarNEW
Association:NHGRI GWAS PheGenI
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:C/T (FWD)
Allele Origin:
Ancestral Allele:T
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:C=0.4262/1609 (1000 Genomes)
C=0.2989/37537 (TOPMED)
HGVS Names
  • CM000685.2:g.12953405C>T
  • NC_000023.10:g.12971524C>T
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 ss283698213 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs5979785 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
ss8270394SC_SNP|NT_011812.10_6157350byFreqfwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact04/17/0310/25/06114Genomicunknown
ss17288961CSHL-HAPMAP|CSHL-HuAA-200402.chrX.NT_011757.13_8938089fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact02/17/0403/04/04120Genomicunknown
ss21006313SSAHASNP|WGSA-200403-chrX.chrX.NT_011757.13_8938089fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact03/19/0403/19/04121Genomicunknown
ss43607147ABI|hCV11532957fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact07/18/0507/18/05126Genomicunknown
ss66495668AFFY|SNP_A-4199388byFreqrev/TA/Gtcattcttcattcggaagaaagaatacataac10/29/0603/31/08127Genomicunknown
ss66845347ILLUMINA|HumanHap300v1.1_rs5979785fwd/TC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact11/09/0611/09/06127Genomicunknown
ss67431411ILLUMINA|HumanHap550v1.1_rs5979785fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact11/14/0611/14/06127Genomicunknown
ss67787878ILLUMINA|HumanHap650Yv1.0_rs5979785fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact11/14/0611/14/06127Genomicunknown
ss69258085PERLEGEN|PGP10906979byFreqfwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact01/30/0703/31/08127Genomicunknown
ss70852645ILLUMINA|HumanHap550v3.0__rs5979785rev/TA/Gagtggatggtaccttcattcttcattcggaagaaagaatacataacaatgatagtaatat04/20/0703/31/08130Genomicunknown
ss71438295ILLUMINA|HumanHap650Yv3.0_rs5979785fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact04/23/0704/23/07127Genomicunknown
ss75889339ILLUMINA|ILMN_Human_1M_rs5979785fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact08/28/0708/29/07129Genomicunknown
ss76318720AFFY|AFFY_6_1M_SNP_A-4199388byFreqrev/TA/Gtcattcttcattcggaagaaagaatacataac08/28/0703/07/10130Genomicunknown
ss79213312ILLUMINA|HumanHap300v2.0_rs5979785fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact04/18/0711/18/07130Genomicunknown
ss84441813KRIBB_YJKIM|KHS711749fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact12/04/0712/07/07130Genomicunknown
ss1127915101000GENOMES|CEU.trio.12.15.2008_3844342_chrX_12881445fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact12/18/0812/18/08130Genomicunknown
ss1144584111000GENOMES|NA19240_2008_12_16_3475055_chrX_12881445fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact12/18/0812/18/08130Genomicunknown
ss115593253ILLUMINA-UK|NA18507_000010660_NCBI36.1_chrX_12881445fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact01/15/0901/15/09130Genomic99 %
ss122495502ILLUMINA|HumanCNV370v1_C_rs5979785fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact04/14/0904/15/09131Genomicunknown
ss154347175ILLUMINA|Human610_Quadv1_B_rs5979785-127_T_R_1501808088rev/TA/Gagtggatggtaccttcattcttcattcggaagaaagaatacataacaatgatagtaatat06/18/0906/20/09131Genomicunknown
ss159523514ILLUMINA|Human660W-Quad_v1_A_rs5979785-128_T_R_1501808088rev/TA/Gagtggatggtaccttcattcttcattcggaagaaagaatacataacaatgatagtaatat07/06/0907/07/09131Genomicunknown
ss161767564ENSEMBL|ENSSNP3096198fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact09/24/0909/25/09131Genomicunknown
ss164474063COMPLETE_GENOMICS|NA19240_36_chrX_12881445fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact09/29/0909/29/09132Genomicunknown
ss172074424ILLUMINA|HumanCNV370-Quadv3_C_rs5979785-127_T_R_1501808088rev/TA/Gagtggatggtaccttcattcttcattcggaagaaagaatacataacaatgatagtaatat10/01/0910/04/09132Genomicunknown
ss173244302AFFY|GenomeWideSNP_5_SNP_A-4199388rev/TA/Gtcattcttcattcggaagaaagaatacataac10/01/0910/03/09132Genomicunknown
ss173955309ILLUMINA|Human1M-Duov3_B_rs5979785-127_T_R_1501808088rev/TA/Gagtggatggtaccttcattcttcattcggaagaaagaatacataacaatgatagtaatat10/01/0910/04/09132Genomicunknown
ss204161215BUSHMAN|BUSHMAN-chrX-12881444fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact02/16/1003/10/10132Genomicunknown
ss208878635BCM-HGSC-SUB|BCM_CMT_1011-3334070fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact03/15/1003/20/10132Genomicunknown
ss255918179BL|SNP5012_X_12881445fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact08/20/1008/20/10134Genomicunknown
ss283698213GMI|GMI_AK_SNP_8018656fwd/C/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact12/16/1012/16/10137Genomicunknown
ss287594958GMI|GMI_NA10851_SNP_3607776fwd/C/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact12/17/1012/17/10138Genomicunknown
ss294520944PJP|SNP_4027302_chrX_12881445fwd/C/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact01/21/1101/21/11134Genomicunknown
ss3413182701000GENOMES|20100804_snps_69974_chrX_12971524fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact03/23/1103/23/11134Genomicunknown
ss482797915ILLUMINA|HumanOmni2.5-4v1_D_kgp22798695-0_T_R_1860348530fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat01/30/1210/28/16137Genomicunknown
ss484344478ILLUMINA|HumanOmni2.5-4v1_B_SNP23-12881445-0_T_R_1650701485fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat01/30/1210/29/16137Genomicunknown
ss491575123EXOME_CHIP|.GWAS._291349_chr_X_12971524fwd/BC/Tatattactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccatccact03/05/1203/06/12137Genomicunknown
ss537326924ILLUMINA|HumanOmni5-4v1_B_rs5979785-131_T_R_1885472898fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat06/22/1208/28/15146Genomicunknown
ss566771549TISHKOFF|snp_chrX_12971524fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat11/22/1211/23/12138Genomicunknown
ss662702412SSMP|X_12971524fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat12/14/1202/14/15138Genomicunknown
ss780073570ILLUMINA|HumanOmni25Exome-8v1_A_kgp22798695-0_T_R_1860348530fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat05/30/1307/09/15146Genomicunknown
ss781881070ILLUMINA|HumanOmni2.5-4v1_H_kgp22798695-0_T_R_1860348530fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat05/30/1307/28/15146Genomicunknown
ss783359184ILLUMINA|HumanOmniExpressExome-8v1_A_exm-rs5979785-131_T_R_1990492941fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat05/31/1306/19/15146Genomicunknown
ss825543830ILLUMINA|HumanCNV370v1_C_rs5979785-126_T_R_IFB1137655776:0fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat06/24/1311/21/14144Genomicunknown
ss835555371ILLUMINA|HumanOmni2.5-8v1_A_kgp22798695-0_T_R_1860348530fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat09/18/1307/28/15146Genomicunknown
ss1082799219JMKIDD_LAB|HGDP_WGS_chrX_12971524fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat07/10/1407/12/14142Genomicunknown
ss1432006476DDI|DDI_rs5979785fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat11/04/1411/05/14144Genomicunknown
ss15535676321000GENOMES|PHASE3_chrX_341456byFreqfwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat08/16/1408/07/15144Genomicunknown
ss1583331596EVA_GENOME_DK|EVA_GENOME_DK_snv_rs5979785fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat02/19/1502/20/15144Genomicunknown
ss1640358054EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_X_12971524_45050058fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat03/04/1503/04/15144Genomicunknown
ss1683352087EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_X_12971524_45050058fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat03/04/1503/04/15144Genomicunknown
ss1752796434ILLUMINA|OmniExpressExome-8v1-1_B_exm-rs5979785-131_T_R_1990492941fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat05/27/1506/09/15146Genomicunknown
ss1917716044ILLUMINA|HumanExome-12v1-1_B_exm-rs5979785-131_T_R_1990492941fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat10/16/1510/16/15147Genomicunknown
ss1939156723WEILL_CORNELL_DGM|SNV:chrX:12971524fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat10/16/1510/19/15147Genomicunknown
ss1945968391ILLUMINA|HumanCoreExome-12v1-0_C_exm-rs5979785-131_T_R_1990492941fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat10/29/1510/29/15147Genomicunknown
ss1958173556ILLUMINA|exm-rs5979785-131_T_R_1990492941fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat11/13/1511/13/15147Genomicunknown
ss1971345694GENOMED|rs5979785fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat02/16/1602/16/16147Genomicunknown
ss2094836641ILLUMINA|Immuno_BeadChip_11419691_B_rs5979785-131_T_R_1863939211fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat09/27/1609/27/16150Genomicunknown
ss2095227482ILLUMINA|InfiniumImmunoArray-24v2-0_A_rs5979785-131_T_R_1863939211fwd/BC/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat09/27/1609/27/16150Genomicunknown
ss2158956045USC_VALOUEV|NC_000023.10:g.12971524C>Tfwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat11/17/1611/17/16150Genomicunknown
ss2315779826HUMAN_LONGEVITY|HLI-X-12953405-C-Tfwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat11/18/1611/18/16150Genomicunknown
ss2629667805SYSTEMSBIOZJU|SYSTEMSBIOZJU_SNV6910157fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat01/06/1701/06/17151Genomicunknown
ss2634940375ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_kgp22798695-0_T_R_18603485fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat02/02/1702/02/17151Genomicunknown
ss2634940376ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_rs5979785-131_T_R_18854728fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat02/02/1702/02/17151Genomicunknown
ss2634940377ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_seq-rs5979785-131_T_R_2130fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat02/02/1702/02/17151Genomicunknown
ss2635201218ILLUMINA|Cancer_BeadChip_11459870_A_rs5979785-128_T_R_1768190158fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat02/02/1702/02/17151Genomicunknown
ss2710084868GRF|rs5979785fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat02/13/1702/13/17151Genomicunknown
ss2976631334GNOMAD|rs5979785fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat05/23/1705/23/17151Genomicunknown
ss2985480965AFFY|Axiom_PsorMich_Affx-34599531fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat05/24/1705/24/17151Genomicunknown
ss2986126887AFFY|Axiom_Smokesc1_Affx-34599531fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat05/24/1705/24/17151Genomicunknown
ss3019652188SWEGEN|NC_000023.10:g.12971524C>Tfwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat05/30/1705/30/17151Genomicunknown
ss3022990872ILLUMINA|MEGA_Consortium_v2_15070954_A2_exm-rs5979785-131_T_R_1990492941fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat06/28/1706/28/17151Genomicunknown
ss3022990873ILLUMINA|MEGA_Consortium_v2_15070954_A2_rs5979785-138_T_R_2264362268fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat06/28/1706/28/17151Genomicunknown
ss3029009426BIOINF_KMB_FNS_UNIBA|X.12953405C>Tfwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat07/05/1707/05/17151Genomicunknown
ss3605662227TOPMED|TOPMed_freeze_5?chrX:12,953,405fwd/C/Tactatcattgttatgtattctttcttccgaatgaagaatgaaggtaccat10/07/1710/07/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs5979785|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=151
 CGTTATGTTG CCCAGGCTAG TCTCAAACTC CTGGACCCAT GTGATCCTCT GGCCTCAAGC
 GATCCTCCAG CCTCAGCCTC AGCCTCCCAA AGTGCTCAGA TTATACCCAG TGTGCCCAGT
 CTATTAATCT GCCTTTTTTG AGTTGATTTT TCAGTAAACC TTCAGAGGGC GAAGGGGAGG
 TTTTCCCTTG GCCCCTACCC TGGATTCAAA TCCTAGCTCC CACTTCCCAA CAATGTGACT
 TTGGGCAAGT CAGGTAACCT GGTTCTCTTC TATAATGTGA GGGAACCATT CTAGCACTTA
 ACCTCAATCA TACTGCATTA CCTTGTTCTG AAGTTTAAAT GAGAAATTCT TAGACTAGCC
 TTCAGCATGT AGTAAAGCAG GCCATAAATG TCAGATATTA TCATAATCTC CAGATTTTCT
 ACAGTGATTC TTGAATGACA TTTAAGATCA GAAACATCCA TGTAATTCTC ATATTACTAT
 CATTGTTATG TATTCTTTCT
 Y
 TCCGAATGAA GAATGAAGGT ACCATCCACT GACACCACAG TCACGAGGTT GGGTCAAGCC
 TTATGACCAC CCTAGAAGCC TAGACAGAAG GGTTCAAAGG CTCTTCCTCT CATATGGGCT
 AGTAATAAAC AGGGTCTCTA ACAGAATAGC GGAAACCTGA GTTGAGCATG TTCATGAGGG
 AGGGGAAGCT GACGCCCACA TCAGCACTTG TTTTCGAAGA GGAGCTGTCT TGGCCCAGAG
 CCGTGGCTCA CGCCTGTAAT CCCAGTATTT TGGGAGGCCA AAGTGGGAGA ATTGCTTGAG
 CCCAAGAGTT CAAGTCTAGC CTGGGCAACA TAGTGAGACC GTGTCTCTAG AAAAAATTTA
 AAAAATTAGA CAGGCATGGT GGTGTGTGCC TGTGATCCCA GCTACTCGGG AGGCTGAGGT
 GGGAAGATTG CTTGAGCCTA GGAGGTCGAG GCTACAGTGA GCTATGATCA CACCACTGCA
 CTCCAGCCTG AGCAACAGAG

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_011812
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.
Source0/C
0/T
C/C
C/T
T/T
HWP0
C
T
ss115593253YRI 2IG 1.00000000 1.00000000
ss1553567632EAS 1008AF 0.872000040.12800001
EUR 1006AF 0.437400010.56259996
AFR 1322AF 0.394099980.60589999
AMR 694AF 0.488500030.51150000
SAS 978AF 0.677900020.32209998
ss161767564ENSEMBL_celera 2IG 1.00000000 1.00000000
ss164474063YRISub-Saharan African 2IG 1.00000000 1.00000000
ss66495668HapMap-CEUEuropean 118IG0.135593220.372881350.016949150.135593220.338983060.150318000.254237290.152542370.59322035
HapMap-HCBAsian 90IG0.400000010.088888890.333333340.17777778 0.367880000.244444440.622222240.13333334
HapMap-JPTAsian 90IG0.422222230.088888890.311111120.17777778 0.301194000.255555570.611111100.13333334
HapMap-YRISub-Saharan African 120IG0.066666670.433333340.016666670.283333330.200000000.010002000.250000000.191666660.55833334
ss69258085HapMap-CEUEuropean 116IG0.137931030.344827590.034482760.137931030.344827590.150318000.241379310.172413800.58620691
HapMap-HCBAsian 88IG0.386363630.090909090.363636370.15909091 0.406570000.238636360.636363630.12500000
HapMap-JPTAsian 90IG0.422222230.088888890.311111120.17777778 0.301194000.255555570.611111100.13333334
HapMap-YRISub-Saharan African 120IG0.066666670.433333340.033333340.266666680.200000000.020040000.250000000.200000000.55000001
ss76318720ICMHP 8IG 0.25000000 0.75000000 0.250000000.75000000
ss8270394HapMap-CEUEuropean 226IG 0.150442480.176991150.672566350.00100000 0.238938050.76106197
HapMap-HCBAsian 84IG 0.738095220.166666670.095238100.01002800 0.821428600.17857143
HapMap-JPTAsian 172IG 0.709302310.162790700.127906980.00100000 0.790697690.20930232
HapMap-YRISub-Saharan African 226IG 0.088495570.247787610.663716790.01002800 0.212389380.78761059
HAPMAP-ASW 98IG 0.081632650.183673470.734693880.02002200 0.173469390.82653064
HAPMAP-CHBAsian 82IG 0.707317050.170731710.121951220.00250100 0.792682950.20731707
HAPMAP-CHD 166IG 0.662650590.168674690.168674690.00100000 0.746987940.25301206
HAPMAP-GIH 176IG 0.420454530.238636360.340909090.00100000 0.539772750.46022728
HAPMAP-LWK 178IG 0.134831460.213483140.651685420.00100000 0.241573040.75842696
HAPMAP-MEX 100IG 0.259999990.280000000.460000010.00499800 0.400000010.60000002
HAPMAP-MKK 286IG 0.181818190.202797200.615384640.00100000 0.283216770.71678323
HAPMAP-TSI 176IG 0.193181810.181818190.625000000.00100000 0.284090910.71590906
ENSEMBL_Venter 2IG 1.00000000 1.00000000

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
Additional Freq. Data
0.489+/-0.0730000ALFRED: 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
byClusterbyFreqwith2hitwithHapMapFreqWith1000GenomeData
DoubleHit found by:  BCM_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

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