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Reference SNP (refSNP) Cluster Report: rs7580332                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:116/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqwith2hitwithHapMapFreqWith1000GenomeData
Association:NHGRI GWAS PheGenI
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=0.3339/1672 (1000 Genomes)
G=0.3669/46077 (TOPMED)
HGVS Names
  • CM000664.2:g.18359378A>G
  • NC_000002.11:g.18540644A>G
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 ss276373622 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs7580332 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
ss11475659WI_SSAHASNP|chr2.NT_015926.13_2182722fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg07/03/0310/25/06116Genomicunknown
ss21734534SSAHASNP|WGSA-200403-chr2.chr2.NT_015926.13_2182722fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg03/20/0403/20/04121Genomicunknown
ss24289355PERLEGEN|afd1234001byFreqfwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg08/10/0409/13/04123Genomicunknown
ss44344433ABI|hCV29229554byFreqfwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg07/18/0511/03/06126Genomicunknown
ss66594820ILLUMINA|HumanHap300v1.1_rs7580332fwd/BA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg11/09/0611/09/06127Genomicunknown
ss67801678ILLUMINA|HumanHap550v1.1_rs7580332fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg11/14/0611/14/06127Genomicunknown
ss67973344ILLUMINA|HumanHap650Yv1.0_rs7580332fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg11/14/0611/15/06127Genomicunknown
ss68390927CSHL-HAPMAP|perlegen:assay:24707.1234001:1byFreqfwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg01/11/0701/16/07127NAunknown
ss70935276ILLUMINA|HumanHap550v3.0__rs7580332fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg04/20/0703/31/08130Genomicunknown
ss71537852ILLUMINA|HumanHap650Yv3.0_rs7580332fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg04/23/0704/23/07127Genomicunknown
ss74921676ILLUMINA|ILMN_Human_1M_rs7580332fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg08/28/0708/29/07129Genomicunknown
ss79261558ILLUMINA|HumanHap300v2.0_rs7580332fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg04/18/0711/18/07130Genomicunknown
ss84683321KRIBB_YJKIM|KHS778608fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg12/04/0712/07/07130Genomicunknown
ss91075872BCMHGSC_JDW|JWB-1208044fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg02/26/0803/01/08129Genomicunknown
ss97017555HUMANGENOME_JCVI|1103658035799fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg03/28/0803/28/08130Genomicunknown
ss103462785BGI|BGI_rs7580332fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg06/06/0806/17/09131Genomicunknown
ss1092732081000GENOMES|CEU.trio.12.15.2008_326597_chr2_18404125fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg12/16/0812/16/08130Genomicunknown
ss122783887ILLUMINA|HumanCNV370v1_C_rs7580332fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg04/14/0904/15/09131Genomicunknown
ss132884587ENSEMBL|ENSSNP1677495fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg12/08/0810/15/09131Genomicunknown
ss138399443ENSEMBL|ENSSNP11972284fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg05/15/0905/17/09131Genomicunknown
ss154431869ILLUMINA|Human610_Quadv1_B_rs7580332-128_T_F_1501853814fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg06/18/0906/20/09131Genomicunknown
ss156764532GMI|GMI_SNP_45900636fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg06/24/0906/25/09131Genomicunknown
ss159606952ILLUMINA|Human660W-Quad_v1_A_rs7580332-128_T_F_1501853814fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg07/06/0907/07/09131Genomicunknown
ss163951571COMPLETE_GENOMICS|NA07022_36_chr2_18404125fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg09/29/0909/29/09132Genomicunknown
ss166225051COMPLETE_GENOMICS|NA20431_36_chr2_18404125fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg09/30/0909/30/09132Genomicunknown
ss172310481ILLUMINA|HumanCNV370-Quadv3_C_rs7580332-128_T_F_1501853814fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg10/01/0910/04/09132Genomicunknown
ss174430772ILLUMINA|Human1M-Duov3_B_rs7580332-128_T_F_1501853814fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg10/01/0910/04/09132Genomicunknown
ss205930626BCM-HGSC-SUB|BCM_CMT_1011-495957fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg03/15/1003/16/10132Genomicunknown
ss209092537ILLUMINA|ALS_iSelect_272541_A_rs7580332-127_T_F_IFB1223202294fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg03/24/1003/24/10132Genomicunknown
ss2191010551000GENOMES|pilot_1_YRI_910738_chr2_18404125fwd/A/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg04/22/1004/22/10132Genomicunknown
ss2310624701000GENOMES|pilot_1_CEU_667099_chr2_18404125fwd/A/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg05/01/1005/01/10132Genomicunknown
ss2386418941000GENOMES|pilot_1_CHB+JPT_526971_chr2_18404125fwd/A/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg05/01/1005/01/10132Genomicunknown
ss252952588BL|SNP22388_2_18404125fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg08/18/1008/18/10134Genomicunknown
ss276373622GMI|GMI_AK_SNP_693789fwd/A/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg12/16/1012/16/10137Genomicunknown
ss284301807GMI|GMI_NA10851_SNP_314573fwd/A/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg12/17/1012/17/10138Genomicunknown
ss292458422PJP|SNP_1964780_chr2_18404125fwd/A/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg01/21/1101/21/11134Genomicunknown
ss491315505EXOME_CHIP|.GWAS._31732_chr_2_18540644fwd/TA/Gatctggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttgggttg03/05/1203/05/12137Genomicunknown
ss537485694ILLUMINA|HumanOmni5-4v1_B_rs7580332-131_T_F_1885470207fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg06/22/1208/28/15146Genomicunknown
ss555395105TISHKOFF|snp_chr2_18540644fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg11/22/1211/23/12138Genomicunknown
ss648972780SSMP|2_18540644fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg12/14/1202/10/15138Genomicunknown
ss780686624ILLUMINA|HumanOmni25Exome-8v1_A_exm-rs7580332-131_T_F_1990494006fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg05/30/1307/09/15142Genomicunknown
ss783360150ILLUMINA|HumanOmniExpressExome-8v1_A_exm-rs7580332-131_T_F_1990494006fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg05/31/1306/19/15142Genomicunknown
ss825592076ILLUMINA|HumanCNV370v1_C_rs7580332-126_T_F_IFB1151456355:0fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg06/24/1311/21/14147Genomicunknown
ss833117933ILLUMINA|Human660W-Quad_v1_C_rs7580332-131_T_F_1864366231fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg09/18/1307/02/15142Genomicunknown
ss833708761ILLUMINA|Human660W-Quad_v1_H_rs7580332-131_T_F_1864366231fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg09/18/1307/02/15142Genomicunknown
ss976550418EVA-GONL|EVA-GONL_rs7580332fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg04/23/1404/23/14142Genomicunknown
ss1068907373JMKIDD_LAB|HGDP_WGS_chr2_18540644fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg07/10/1407/10/14142Genomicunknown
ss12961406971000GENOMES|PHASE3_V1_7085884fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg08/16/1408/16/14142Genomicunknown
ss1397284437HAMMER_LAB|HAMMER_LAB_rs7580332fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg09/30/1409/30/14146Genomicunknown
ss1428497173DDI|DDI_rs7580332fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg11/04/1411/04/14144Genomicunknown
ss1578765239EVA_GENOME_DK|EVA_GENOME_DK_snv_rs7580332fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg02/19/1502/20/15144Genomicunknown
ss1585951848EVA_DECODE|EVA_DECODE_2_18404125_153736_rs7580332fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg03/02/1503/02/15144Genomicunknown
ss1602933829EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_2_18540644_3912608fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg03/04/1503/04/15144Genomicunknown
ss1645927862EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_2_18540644_3912608fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg03/04/1503/04/15144Genomicunknown
ss1712435706EVA_SVP|EVA_SVP_130258fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg03/12/1503/12/15144Genomicunknown
ss1752328674ILLUMINA|OmniExpressExome-8v1-1_B_exm-rs7580332-131_T_F_1990494006fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg05/27/1506/09/15146Genomicunknown
ss1917746187ILLUMINA|HumanExome-12v1-1_B_exm-rs7580332-131_T_F_1990494006fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg10/16/1510/16/15147Genomicunknown
ss1919784052WEILL_CORNELL_DGM|SNV:chr2:18540644fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg10/16/1510/16/15147Genomicunknown
ss1946033371ILLUMINA|HumanCoreExome-12v1-0_C_exm-rs7580332-131_T_F_1990494006fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg10/29/1510/29/15147Genomicunknown
ss1958393797ILLUMINA|exm-rs7580332-131_T_F_1990494006fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg11/13/1511/13/15147Genomicunknown
ss1968708584GENOMED|rs7580332fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg02/16/1602/16/16147Genomicunknown
ss2020418282JJLAB|SNP920837fwd/TA/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg08/29/1608/30/16149Genomicunknown
ss2148463156USC_VALOUEV|NC_000002.11:g.18540644A>Gfwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg11/17/1611/17/16150Genomicunknown
ss2227989135HUMAN_LONGEVITY|HLI-2-18359378-A-Gfwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg11/18/1611/18/16150Genomicunknown
ss2393900806TOPMED|2_18540644_A/Gfwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg11/19/1611/19/16150Genomicunknown
ss2624726394SYSTEMSBIOZJU|SYSTEMSBIOZJU_SNV587362fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg01/06/1701/06/17151Genomicunknown
ss2635086835ILLUMINA|Cancer_BeadChip_11459870_A_rs7580332-128_T_F_1782930661fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg02/02/1702/02/17151Genomicunknown
ss2703022552GRF|rs7580332fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg02/13/1702/13/17151Genomicunknown
ss2770377294GNOMAD|rs7580332fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg05/17/1705/17/17151Genomicunknown
ss2985160393AFFY|Axiom_PsorMich_Affx-18625609fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg05/24/1705/24/17151Genomicunknown
ss2989071856SWEGEN|NC_000002.11:g.18540644A>Gfwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg05/30/1705/30/17151Genomicunknown
ss3021945711ILLUMINA|MEGA_Consortium_v2_15070954_A2_exm-rs7580332-131_T_F_1990494006fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg06/28/1706/28/17151Genomicunknown
ss3023976253BIOINF_KMB_FNS_UNIBA|2.18359378A>Gfwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg07/05/1707/05/17151Genomicunknown
ss3300772996TOPMED|TOPMed_freeze_5?chr2:18,359,378fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg10/02/1710/02/17151Genomicunknown
ss3344103360CSHL|rs7580332fwd/A/Ggaaggtatggttgtccttgctgtggaagaaagtttaatcagtcttacttg10/02/1710/02/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs7580332|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=151
 GTGCTGGGAT TACAGGCGTG AGCCATCATG CCCAGCCAAC ATGCAGTCAA CATTGATTGT
 CTTCATTACT TTAAGATATG TGCATCTTGC ATTCACCTAA CACATCCCAT AGTTAGTGTT
 GTTTTACTGA AGAAAAAGAT AAAATAGGAT ATGGTGAAAT TTTGTGCAAA CCTGAGAAAT
 TACTGCTATA ATCTGGGTTC TTTCCTTGAG ATTTATTCAA AGTATCCAAA AAGAAGAAAA
 TACATACATT GGGAGGAACT TTATTATCCA TCGATAAGGC AAAAAAGGCT TATACTCTTT
 GCCAGTAACT GCAACAATTA TTCCCCAAAT CATTAAATTA TATTGCTGAA AGTCACAGTG
 AAATGATCCT TAGCTCTGAA GCATAAAAAT TCATAAAATT ATCACAAAAA TTAAAAGGAA
 TCCTTCTTTT CTAGGAAAAA AACTCGTAAC TACAAAGTGA GAATATTCCT ATCTGGAAGG
 TATGGTTGTC CTTGCTGTGG
 R
 AAGAAAGTTT AATCAGTCTT ACTTGGGTTG AAACCATTCA AGGGCACTCC TAGGTGGGTG
 GGTGATGAGG TGAGGTTGAG AATACAACAG ATAAATGGCA TCTTGCCCCA AACTCCATCT
 CCCTTGTCTT CTCTGAGACA GGGCCAACCC AGGTTACCAG GTGGTTGGGA CAATGTTCTA
 CTCTGGAATG CTTTTTTCCC AGATTCAATA CTACCTGCAG AGAAAGTCAT ACAAGAACTT
 CTGTGATGTT TGTATCCAGT GATGTTAGGA CATTTCTGAA GTCCCAAGCA TGGGTCAGGG
 CCATGAAAGC TATGTGGCTT GGCTTGTCAT CGGTGTTCCT TAATTAGACA GATTTGCTAG
 AAGATTCTTC GGAGATGAGT TCTCTTGCCC ATGCGGTGGG TTGTCTAATT CCAAGTTTAA
 GTTGGACCAT TAATCAATCT ATGGCTGGAG ACTGTTGTCC ATCTCTCTAT CTTGTAATTC
 TTTTTTCATT CCTCTTTCTA

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_015926 ABBA01018504
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
ss1296140697EAS 1008AF 0.658699990.34129998
EUR 1006AF 0.600399970.39960000
AFR 1322AF 0.761700030.23830000
AMR 694AF 0.582099970.41790003
SAS 978AF 0.671799960.32820001
ss132884587ENSEMBL_Venter 2IG 1.00000000 0.500000000.50000000
ss138399443ENSEMBL_Watson 2IG 1.00000000 0.500000000.50000000
ss163951571CEUEuropean 2IG 1.00000000 0.500000000.50000000
ss166225051PGP 2IG 1.00000000 0.500000000.50000000
ss219101055pilot_1_YRI_low_coverage_panel 118AF 0.745762710.25423729
ss231062470pilot_1_CEU_low_coverage_panel 120AF 0.574999990.42500001
ss238641894pilot_1_CHB+JPT_low_coverage_panel 120AF 0.641666650.35833332
ss24289355AFD_EUR_PANELEuropean 48IG0.333333340.541666690.125000000.527089000.604166690.39583334
AFD_AFR_PANELAfrican American 44IG0.545454560.363636370.090909090.751830000.727272750.27272728
AFD_CHN_PANELAsian 48IG0.541666690.333333340.125000000.371093000.708333310.29166666
ss44344433HapMap-CEUEuropean 226IG0.300884960.504424750.194690271.000000000.553097370.44690266
HapMap-HCBAsian 86IG0.372093020.511627910.116279070.583882000.627906980.37209302
HapMap-JPTAsian 172IG0.488372090.441860470.069767450.527089000.709302310.29069766
HapMap-YRISub-Saharan African 224IG0.571428600.339285700.089285720.250592000.741071400.25892857
HAPMAP-ASW 98IG0.714285730.265306120.020408161.000000000.846938790.15306123
HAPMAP-CHBAsian 80IG0.400000010.474999990.125000001.000000000.637499990.36250001
HAPMAP-CHD 170IG0.423529420.376470600.200000000.099721000.611764730.38823530
HAPMAP-GIH 176IG0.465909090.465909090.068181820.317310000.698863630.30113637
HAPMAP-LWK 180IG0.644444470.300000010.055555560.479500000.794444440.20555556
HAPMAP-MEX 100IG0.319999990.500000000.180000011.000000000.569999990.43000001
HAPMAP-MKK 282IG0.446808520.453900690.099290780.751830000.673758860.32624114
HAPMAP-TSI 176IG0.443181810.431818190.125000000.751830000.659090940.34090909
ss97017555J. Craig Venter 2IG 1.00000000 0.500000000.50000000

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
Additional Freq. Data
0.445+/-0.1570000ALFRED: 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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