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Reference SNP (refSNP) Cluster Report: rs16984239                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:123/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqWith1000GenomeData
Citation:PubMedLitVarNEW
Association:NHGRI GWAS PheGenI
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:A/C (FWD)
Allele Origin:
Ancestral Allele:C
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:A=0.1448/725 (1000 Genomes)
A=0.1462/18360 (TOPMED)
HGVS Names
  • CM000664.2:g.18053180C>A
  • NC_000002.11:g.18234446C>A
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 ss276372425 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs16984239 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
ss24155110PERLEGEN|afd1233527byFreqfwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag08/10/0409/13/04123Genomicunknown
ss66064180AFFY|SNP_A-1865197byFreqfwd/TA/Ctccataatggtaagtcacatctaagtctcagt10/27/0603/31/08127Genomicunknown
ss66802294ILLUMINA|HumanHap300v1.1_rs16984239fwd/BA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag11/09/0611/09/06127Genomicunknown
ss67164081ILLUMINA|HumanHap550v1.1_rs16984239fwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag11/14/0611/14/06127Genomicunknown
ss67515351ILLUMINA|HumanHap650Yv1.0_rs16984239fwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag11/14/0611/14/06127Genomicunknown
ss70449481ILLUMINA|HumanHap300v2.0_rs16984239fwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag04/18/0711/18/07127Genomicunknown
ss70648086ILLUMINA|HumanHap550v3.0__rs16984239rev/BG/Tctagcaaggggtgtactgagacttagatgtgacttaccattatggaaaagcagaagaaaa04/20/0703/30/08130Genomicunknown
ss71203766ILLUMINA|HumanHap650Yv3.0_rs16984239fwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag04/23/0704/23/07127Genomicunknown
ss75854630ILLUMINA|ILMN_Human_1M_rs16984239fwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag08/28/0708/29/07129Genomicunknown
ss75986469AFFY|AFFY_6_1M_SNP_A-1865197fwd/TA/Ctccataatggtaagtcacatctaagtctcagt08/28/0708/29/07129Genomicunknown
ss85345731KRIBB_YJKIM|KHS971114fwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag12/04/0712/09/07130Genomicunknown
ss121781210ILLUMINA|HumanCNV370v1_C_rs16984239fwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag04/14/0904/14/09131Genomicunknown
ss153591612ILLUMINA|Human610_Quadv1_B_rs16984239-128_B_R_1501693147rev/BG/Tctagcaaggggtgtactgagacttagatgtgacttaccattatggaaaagcagaagaaaa06/18/0906/19/09131Genomicunknown
ss159301297ILLUMINA|Human660W-Quad_v1_A_rs16984239-128_B_R_1501693147rev/BG/Tctagcaaggggtgtactgagacttagatgtgacttaccattatggaaaagcagaagaaaa07/06/0907/06/09131Genomicunknown
ss160406591ILLUMINA|HumanOmni1-Quad_v1-0_B_rs16984239-128_B_R_1501693147rev/BG/Tctagcaaggggtgtactgagacttagatgtgacttaccattatggaaaagcagaagaaaa08/04/0910/02/09131Genomicunknown
ss163947797COMPLETE_GENOMICS|NA07022_36_chr2_18097927fwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag09/29/0909/29/09132Genomicunknown
ss170047304AFFY|GenomeWideSNP_5_SNP_A-1865197fwd/TA/Ctccataatggtaagtcacatctaagtctcagt10/01/0910/01/09132Genomicunknown
ss170731704ILLUMINA|HumanCNV370-Quadv3_C_rs16984239-128_B_R_1501693147rev/BG/Tctagcaaggggtgtactgagacttagatgtgacttaccattatggaaaagcagaagaaaa10/01/0910/03/09132Genomicunknown
ss172692155ILLUMINA|Human1M-Duov3_B_rs16984239-128_B_R_1501693147rev/BG/Tctagcaaggggtgtactgagacttagatgtgacttaccattatggaaaagcagaagaaaa10/01/0910/02/09132Genomicunknown
ss205598459BCM-HGSC-SUB|BCM_CMT_1011-278359fwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag03/15/1003/16/10132Genomicunknown
ss209086609ILLUMINA|ALS_iSelect_272541_A_rs16984239-127_B_R_IFB1223194853rev/BG/Tctagcaaggggtgtactgagacttagatgtgacttaccattatggaaaagcagaagaaaa03/24/1003/24/10132Genomicunknown
ss2190993861000GENOMES|pilot_1_YRI_909069_chr2_18097927fwd/A/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag04/22/1004/22/10132Genomicunknown
ss2310610921000GENOMES|pilot_1_CEU_665721_chr2_18097927fwd/A/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag05/01/1005/01/10132Genomicunknown
ss2386409231000GENOMES|pilot_1_CHB+JPT_526000_chr2_18097927fwd/A/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag05/01/1005/01/10132Genomicunknown
ss276372425GMI|GMI_AK_SNP_692592fwd/A/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag12/16/1012/16/10137Genomicunknown
ss480133009ILLUMINA|HumanOmni2.5-4v1_B_rs16984239-128_B_R_1767726769fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt01/30/1210/28/16137Genomicunknown
ss480142064ILLUMINA|HumanOmniExpress-12v1_C_rs16984239-131_B_R_1857683788fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt01/30/1210/27/16137Genomicunknown
ss480843213ILLUMINA|HumanOmni1-Quad_v1-0_C_rs16984239-131_B_R_1865592325fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt01/30/1208/28/15146Genomicunknown
ss484864490ILLUMINA|HumanOmni2.5-4v1_D_rs16984239-131_B_R_1857683788fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt01/30/1210/28/16137Genomicunknown
ss491315502EXOME_CHIP|.GWAS._31729_chr_2_18234446fwd/TA/Cttttcttctgcttttccataatggtaagtcacatctaagtctcagtacaccccttgctag03/05/1203/05/12137Genomicunknown
ss536928988ILLUMINA|HumanOmni5-4v1_B_rs16984239-131_B_R_1885470131fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt06/22/1208/28/15146Genomicunknown
ss648970879SSMP|2_18234446fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt12/14/1202/10/15138Genomicunknown
ss778823666ILLUMINA|HumanOmni25Exome-8v1_A_rs16984239-131_B_R_1865592325fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt05/30/1307/09/15146Genomicunknown
ss780682302ILLUMINA|HumanOmni25Exome-8v1_A_exm-rs16984239-131_B_R_1990480001fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt05/30/1307/09/15146Genomicunknown
ss782878669ILLUMINA|HumanOmni2.5-4v1_H_rs16984239-131_B_R_1857683788fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt05/30/1307/28/15146Genomicunknown
ss783355648ILLUMINA|HumanOmniExpressExome-8v1_A_exm-rs16984239-131_B_R_1990480001fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt05/31/1306/19/15146Genomicunknown
ss783842504ILLUMINA|HumanOmniExpressExome-8v1_A_rs16984239-131_B_R_1885470131fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt05/31/1306/19/15146Genomicunknown
ss825418214ILLUMINA|HumanCNV370v1_C_rs16984239-123_B_R_IFB1156314460:0fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt06/24/1311/21/14144Genomicunknown
ss832132962ILLUMINA|HumanOmniExpress-12v1_H_rs16984239-131_B_R_1857683788fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt09/17/1306/18/15146Genomicunknown
ss834284041ILLUMINA|HumanOmni2.5-8v1_A_rs16984239-131_B_R_1865592325fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt09/18/1307/28/15146Genomicunknown
ss976547408EVA-GONL|EVA-GONL_rs16984239fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt04/23/1404/23/14142Genomicunknown
ss1068905136JMKIDD_LAB|HGDP_WGS_chr2_18234446fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt07/10/1407/10/14142Genomicunknown
ss12961309861000GENOMES|PHASE3_V1_7075791fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt08/16/1408/16/14142Genomicunknown
ss1397284306HAMMER_LAB|HAMMER_LAB_rs16984239fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt09/30/1409/30/14146Genomicunknown
ss1578763843EVA_GENOME_DK|EVA_GENOME_DK_snv_rs16984239fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt02/19/1502/20/15144Genomicunknown
ss1585948869EVA_DECODE|EVA_DECODE_2_18097927_150757_rs16984239fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt03/02/1503/02/15144Genomicunknown
ss1602928513EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_2_18234446_3906800fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt03/04/1503/04/15144Genomicunknown
ss1645922546EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_2_18234446_3906800fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt03/04/1503/04/15144Genomicunknown
ss1712435455EVA_SVP|EVA_SVP_130007fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt03/12/1503/12/15144Genomicunknown
ss1752327785ILLUMINA|OmniExpressExome-8v1-1_B_exm-rs16984239-131_B_R_1990480001fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt05/27/1506/09/15146Genomicunknown
ss1752327786ILLUMINA|OmniExpressExome-8v1-1_B_rs16984239-131_B_R_2087475646fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt05/27/1506/09/15146Genomicunknown
ss1917746184ILLUMINA|HumanExome-12v1-1_B_exm-rs16984239-131_B_R_1990480001fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt10/16/1510/16/15147Genomicunknown
ss1919781002WEILL_CORNELL_DGM|SNV:chr2:18234446fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt10/16/1510/16/15147Genomicunknown
ss1946033322ILLUMINA|HumanCoreExome-12v1-0_C_exm-rs16984239-131_B_R_1990480001fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt10/29/1510/29/15147Genomicunknown
ss1946033323ILLUMINA|HumanCoreExome-12v1-0_C_rs16984239-131_B_R_2087475646fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt10/29/1510/29/15147Genomicunknown
ss1958393603ILLUMINA|exm-rs16984239-131_B_R_1990480001fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt11/13/1511/13/15147Genomicunknown
ss1958393604ILLUMINA|rs16984239-131_B_R_1885470131fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt11/13/1511/13/15147Genomicunknown
ss1968707657GENOMED|rs16984239fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt02/16/1602/16/16147Genomicunknown
ss2020416574JJLAB|SNP919129fwd/TA/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt08/29/1608/30/16149Genomicunknown
ss2148461298USC_VALOUEV|NC_000002.11:g.18234446C>Afwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt11/17/1611/17/16150Genomicunknown
ss2227969846HUMAN_LONGEVITY|HLI-2-18053180-C-Afwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt11/18/1611/18/16150Genomicunknown
ss2393881478TOPMED|2_18234446_C/Afwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt11/19/1611/19/16150Genomicunknown
ss2624725554SYSTEMSBIOZJU|SYSTEMSBIOZJU_SNV586387fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt01/06/1701/06/17151Genomicunknown
ss2633579426ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_SoL-rs16984239-131_B_R_213fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt02/02/1702/02/17151Genomicunknown
ss2633579427ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_rs16984239-131_B_R_2087475fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt02/02/1702/02/17151Genomicunknown
ss2633579428ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_seq-rs16984239-131_B_R_213fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt02/02/1702/02/17151Genomicunknown
ss2703020849GRF|rs16984239fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt02/13/1702/13/17151Genomicunknown
ss2710891698ILLUMINA|Consortium-OncoArray_15047405_A_rs16984239-131_B_R_2087475646fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt03/22/1703/22/17151Genomicunknown
ss2770351197GNOMAD|rs16984239fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt05/17/1705/17/17151Genomicunknown
ss2985160343AFFY|Axiom_PsorMich_Affx-18588664fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt05/24/1705/24/17151Genomicunknown
ss2989067818SWEGEN|NC_000002.11:g.18234446C>Afwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt05/30/1705/30/17151Genomicunknown
ss3021945484ILLUMINA|MEGA_Consortium_v2_15070954_A2_exm-rs16984239-131_B_R_1990480001fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt06/28/1706/28/17151Genomicunknown
ss3021945485ILLUMINA|MEGA_Consortium_v2_15070954_A2_rs16984239-138_B_R_2264356771fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt06/28/1706/28/17151Genomicunknown
ss3023975349BIOINF_KMB_FNS_UNIBA|2.18053180C>Afwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt07/05/1707/05/17151Genomicunknown
ss3300713397TOPMED|TOPMed_freeze_5?chr2:18,053,180fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt10/02/1710/02/17151Genomicunknown
ss3344101703CSHL|rs16984239fwd/A/Cttctgcttttccataatggtaagtcacatctaagtctcagtacacccctt10/02/1710/02/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs16984239|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='A/C'|mol=Genomic|build=151
 CTTGGGAGCA AGAGGTGAGG AGGATGCCCT ATTCTGAACA GTAGTAATGG CAGATGGTGG
 GTGGGCTAGA ACGATGTCCT CTTGCTGTAG AAACACTGCA TTTCCAAGAC CCCACTGGGC
 CTCCCAGTAT AAATCGTGTT TCCAGGATGC TCAGGGGACC CATCTTCAAG ATTAACCTCT
 TACTGAAGCT CCAGGCAGAT TCCTATAGAA TTACCAAGGA GATTCCTATA GAACATCTAA
 ACTGTCCAAC AAAAGATTTT AAGGTATGGT GAAAAAGAGT GATGGTGGCC AGAGAATGGT
 GCTGCAGAGA AGGTATAATA CCTACACTCC TTTCAAGGGA GGCAAACTAA AATACTATGA
 GGTGAAAACC AACTGATGCA GGAACAAGCA GATCAACTCC AGCTTTCATT AGAAGCAGAG
 CCAACTTGAA ATCTGCATCA TATATGGCTT TAATTTTAAG CTAAGTTCTG TTTTCTTCTG
 CTTTTCCATA ATGGTAAGTC
 M
 ACATCTAAGT CTCAGTACAC CCCTTGCTAG CCATAAGACA ACCATTGGAG CACAGGAAAC
 CCATTCATAA GTTGGTTGAC TTGGTGTAGT GACAGACAAA GAAGGGGTGT TAATAACCCC
 TAAGTGATAG CCCCCAAAGA ATAATGCTAC TTCCCCCCTC AATAAAGGCC TCCAACCATG
 ACCACGCTCT AATCTCTGGA ACCTGGAAAT ATGTTATCTT ACTTGGCAAA ATACACTTTG
 TAGGTGTGTT TATAGTTAAG GACCTGAATA GGTGAAGATT ATCCTGTTAT CCAGGTAATC
 CCAGGCTAAT CACCAAATCC TTAAAAGTAA AGAATATTTC AGGTTTCAGA GAACCAGAGG
 GACAGCAGCA TGAGAAAGAC TCAACCTACC ATTGCTGGGT TTGAAGATGG AGCCATGGAT
 TACAGGCAGC CTTTAGAAGC TGAAAAAGGC AAGGGCACAT CTACAAAGGT GTATTAGTCC
 ATTATCATGC TGCTGATAAA

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NC_000002.6
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/C
C/C
HWPA
C
ss1296130986EAS 1008AF 0.281700020.71829998
EUR 1006AF 0.197800000.80219996
AFR 1322AF 0.018200000.98179996
AMR 694AF 0.141199990.85879999
SAS 978AF 0.122700010.87729996
ss163947797CEUEuropean 2IG1.00000000 1.00000000
ss219099386pilot_1_YRI_low_coverage_panel 118AF 0.033898310.96610171
ss231061092pilot_1_CEU_low_coverage_panel 120AF 0.183333340.81666666
ss238640923pilot_1_CHB+JPT_low_coverage_panel 120AF 0.300000010.69999999
ss24155110AFD_EUR_PANELEuropean 48IG0.083333340.166666670.750000000.099721000.166666670.83333331
AFD_AFR_PANELAfrican American 46IG 0.173913050.826086941.000000000.086956520.91304350
AFD_CHN_PANELAsian 48IG0.083333340.250000000.666666690.250592000.208333330.79166669
HapMap-CEUEuropean 226IG0.035398230.380530980.584070800.371093000.225663720.77433628
HapMap-HCBAsian 86IG0.139534890.372093020.488372090.317310000.325581400.67441863
HapMap-JPTAsian 172IG0.058139540.383720930.558139561.000000000.250000000.75000000
HapMap-YRISub-Saharan African 226IG 0.026548670.973451321.000000000.013274340.98672569
HAPMAP-ASW 98IG 0.081632650.918367331.000000000.040816330.95918369
HAPMAP-CHBAsian 82IG0.121951220.414634140.463414640.751830000.329268310.67073172
HAPMAP-CHD 170IG0.070588240.517647090.411764710.150222000.329411770.67058825
HAPMAP-GIH 176IG0.011363640.250000000.738636370.583882000.136363640.86363637
HAPMAP-LWK 180IG 0.022222220.977777781.000000000.011111110.98888886
HAPMAP-MEX 100IG 0.340000000.660000030.438578000.170000000.82999998
HAPMAP-MKK 286IG0.006993010.076923080.916083930.200325000.045454550.95454544
HAPMAP-TSI 176IG0.011363640.375000000.613636370.099721000.198863640.80113637
ss66064180HapMap-CEUEuropean 118IG0.033898310.305084740.661016941.000000000.186440680.81355929
HapMap-HCBAsian 90IG0.133333340.377777790.488888890.371093000.322222230.67777777
HapMap-JPTAsian 90IG0.022222220.377777790.600000020.371093000.211111110.78888887
HapMap-YRISub-Saharan African 120IG 0.050000000.949999991.000000000.025000000.97500002
ss75986469ICMHP 10IG 0.200000000.80000001 0.100000000.89999998

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
Additional Freq. Data
0.248+/-0.2500000ALFRED: 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
byClusterbyFreqWith1000GenomeDataUNKNOWNUNKNOWNUNKNOWN

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