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Reference SNP (refSNP) Cluster Report: rs11250168                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:120/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqwith2hitwithHapMapFreqWith1000GenomeData
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:C/G/T (FWD)
Allele Origin:
Ancestral Allele:G
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:T=0.2612/1308 (1000 Genomes)
T=0.2202/27654 (TOPMED)
HGVS Names
  • CM000670.2:g.11833633G>C
  • CM000670.2:g.11833633G>T
  • NC_000008.10:g.11691142G>T
  • NC_000008.11:g.11833633G>C
  • NC_000008.11:g.11833633G>T
  • NM_001287742.1:c.1032+1963G>C
  • NM_001287742.1:c.1032+1963G>T
  • NM_001287743.1:c.1032+1963G>C
  • NM_001287743.1:c.1032+1963G>T
  • NM_001287744.1:c.840+1963G>C
  • NM_001287744.1:c.840+1963G>T
  • NM_001287745.1:c.840+1963G>C
  • NM_001287745.1:c.840+1963G>T
  • NM_001287747.1:c.840+1963G>C
  • NM_001287747.1:c.840+1963G>T
  • NM_001287748.1:c.840+1963G>C
  • NM_001287748.1:c.840+1963G>T
  • NM_001287749.1:c.840+1963G>C
  • NM_001287749.1:c.840+1963G>T
  • NM_001287750.1:c.1209+1963G>C
  • NM_001287750.1:c.1209+1963G>T
  • NM_001287751.1:c.777+1963G>C
  • NM_001287751.1:c.777+1963G>T
  • NM_001287756.1:c.531+1963G>C
  • NM_001287756.1:c.531+1963G>T
  • NM_004462.4:c.1032+1963G>C
  • NM_004462.4:c.1032+1963G>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 ss279685014 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs11250168 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
ss17978747CSHL-HAPMAP|CSHL-HuCC-200402.chr8.NT_077531.3_4166492fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg02/19/0410/26/06120Genomicunknown
ss19757892CSHL-HAPMAP|CSHL-HuDD-200402.chr8.NT_077531.3_4166492fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg02/20/0403/04/04120Genomicunknown
ss22700182SSAHASNP|WGSA-200403-chr8.chr8.NT_077531.3_4166492fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg03/21/0403/21/04121Genomicunknown
ss43287234ABI|hCV31687811byFreqfwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg07/18/0511/03/06126Genomicunknown
ss66603369ILLUMINA|HumanHap300v1.1_rs11250168fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg11/09/0611/09/06127Genomicunknown
ss66929217ILLUMINA|HumanHap550v1.1_rs11250168fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg11/14/0611/14/06127Genomicunknown
ss67085552ILLUMINA|HumanHap650Yv1.0_rs11250168fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg11/14/0611/14/06127Genomicunknown
ss70393051ILLUMINA|HumanHap300v2.0_rs11250168fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg04/18/0711/18/07127Genomicunknown
ss70527194ILLUMINA|HumanHap550v3.0__rs11250168rev/TA/Ccatttattcacaaaaacagggctcagccaatgtagactgcccaccctcgccctcaaacta04/20/0703/30/08130Genomicunknown
ss71057304ILLUMINA|HumanHap650Yv3.0_rs11250168fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg04/23/0704/23/07127Genomicunknown
ss75544778ILLUMINA|ILMN_Human_1M_rs11250168fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg08/28/0708/29/07129Genomicunknown
ss83993727HGSV|Cor18555_SNV_20070510.chr8_11728551fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg11/27/0712/06/07130Genomicunknown
ss85095081KRIBB_YJKIM|KHS897379fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg12/04/0712/08/07130Genomicunknown
ss93833084BCMHGSC_JDW|JWB-2424320fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg02/26/0803/05/08129Genomicunknown
ss98049029HUMANGENOME_JCVI|1103652244281fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg03/30/0803/31/08130Genomicunknown
ss104502485BGI|BGI_rs11250168fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg06/08/0806/18/09131Genomicunknown
ss1128184991000GENOMES|CEU.trio.12.15.2008_1927823_chr8_11728551fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg12/18/0812/18/08130Genomicunknown
ss1149591261000GENOMES|NA19240_2008_12_16_1737797_chr8_11728551fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg12/19/0812/19/08130Genomicunknown
ss121466427ILLUMINA|HumanCNV370v1_C_rs11250168fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg04/14/0904/14/09131Genomicunknown
ss134552615ENSEMBL|ENSSNP2726777fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg12/08/0810/15/09131Genomicunknown
ss143253598ENSEMBL|ENSSNP13422837fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg06/05/0906/06/09131Genomicunknown
ss152977555ILLUMINA|Human610_Quadv1_B_rs11250168-128_T_R_1501626449rev/TA/Ccatttattcacaaaaacagggctcagccaatgtagactgcccaccctcgccctcaaacta06/18/0906/19/09131Genomicunknown
ss155998817GMI|GMI_SNP_129530264fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg06/24/0906/24/09131Genomicunknown
ss159173232ILLUMINA|Human660W-Quad_v1_A_rs11250168-128_T_R_1501626449rev/TA/Ccatttattcacaaaaacagggctcagccaatgtagactgcccaccctcgccctcaaacta07/06/0907/06/09131Genomicunknown
ss163927789COMPLETE_GENOMICS|NA19240_36_chr8_11728551fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg09/29/0909/29/09132Genomicunknown
ss166222400COMPLETE_GENOMICS|NA20431_36_chr8_11728551fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg09/30/0909/30/09132Genomicunknown
ss169843821ILLUMINA|HumanCNV370-Quadv3_C_rs11250168-128_T_R_1501626449rev/TA/Ccatttattcacaaaaacagggctcagccaatgtagactgcccaccctcgccctcaaacta10/01/0910/02/09132Genomicunknown
ss171220551ILLUMINA|Human1M-Duov3_B_rs11250168-128_T_R_1501626449rev/TA/Ccatttattcacaaaaacagggctcagccaatgtagactgcccaccctcgccctcaaacta10/01/0910/01/09132Genomicunknown
ss2235358501000GENOMES|pilot_1_YRI_5345533_chr8_11728551fwd/G/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg04/22/1004/22/10132Genomicunknown
ss2343151531000GENOMES|pilot_1_CEU_3919782_chr8_11728551fwd/G/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg05/01/1005/01/10132Genomicunknown
ss2411978261000GENOMES|pilot_1_CHB+JPT_3082903_chr8_11728551fwd/G/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg05/01/1005/01/10132Genomicunknown
ss244272275ILLUMINA|CVDSNP55v1_A_rs11250168rev/TA/Ccatttattcacaaaaacagggctcagccaatgtagactgcccaccctcgccctcaaacta06/10/1006/10/10132Genomicunknown
ss254095361BL|SNP25134_8_11728551fwd/BG/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg08/19/1008/19/10134Genomicunknown
ss279685014GMI|GMI_AK_SNP_4005267fwd/G/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg12/16/1012/16/10137Genomicunknown
ss285789480GMI|GMI_NA10851_SNP_1802253fwd/G/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg12/17/1012/17/10138Genomicunknown
ss294214350PJP|SNP_3720708_chr8_11728551fwd/G/Ttagtttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaataaatg01/21/1101/21/11134Genomicunknown
ss480085730ILLUMINA|HumanOmni2.5-4v1_D_kgp12527549-0_B_F_1809089433fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat01/30/1210/28/16137Genomicunknown
ss485525378ILLUMINA|HumanOmni2.5-4v1_B_SNP8-11728551-0_B_F_1621184483fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat01/30/1210/29/16137Genomicunknown
ss533532333ILLUMINA|HumanOmni5-4v1_B_kgp12527549-0_B_F_1809089433fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat06/22/1208/29/15146Genomicunknown
ss560542249TISHKOFF|snp_chr8_11691142fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat11/22/1211/23/12138Genomicunknown
ss654971878SSMP|8_11691142fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat12/14/1202/12/15138Genomicunknown
ss779707795ILLUMINA|HumanOmni25Exome-8v1_A_kgp12527549-0_B_F_1809089433fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat05/30/1307/10/15146Genomicunknown
ss781143222ILLUMINA|HumanOmni2.5-4v1_H_kgp12527549-0_B_F_1809089433fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat05/30/1307/29/15146Genomicunknown
ss825362446ILLUMINA|HumanCNV370v1_C_rs11250168-126_T_R_IFB1152666883:0fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat06/24/1311/21/14144Genomicunknown
ss835182059ILLUMINA|HumanOmni2.5-8v1_A_kgp12527549-0_B_F_1809089433fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat09/18/1307/29/15146Genomicunknown
ss985182332EVA-GONL|EVA-GONL_rs11250168fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat04/23/1404/25/14142Genomicunknown
ss1075266713JMKIDD_LAB|HGDP_WGS_chr8_11691142fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat07/10/1407/11/14142Genomicunknown
ss13285773321000GENOMES|PHASE3_V1_40879532fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat08/16/1408/16/14142Genomicunknown
ss1431409712DDI|DDI_rs11250168fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat11/04/1411/05/14144Genomicunknown
ss1582553593EVA_GENOME_DK|EVA_GENOME_DK_snv_rs11250168fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat02/19/1502/20/15144Genomicunknown
ss1594769831EVA_DECODE|EVA_DECODE_8_11728551_148540_rs11250168fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat03/02/1503/03/15144Genomicunknown
ss1619960476EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_8_11691142_22610751fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat03/04/1503/04/15144Genomicunknown
ss1662954509EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_8_11691142_22610751fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat03/04/1503/04/15144Genomicunknown
ss1713014224EVA_SVP|EVA_SVP_708591fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat03/12/1503/12/15144Genomicunknown
ss1805393100HAMMER_LAB|Hsieh_4407172fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat07/15/1507/16/15146Genomicunknown
ss1928465412WEILL_CORNELL_DGM|SNV:chr8:11691142fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat10/16/1510/17/15147Genomicunknown
ss1970905372GENOMED|rs11250168fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat02/16/1602/16/16147Genomicunknown
ss2024926528JJLAB|SNP5429083fwd/BG/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat08/29/1608/30/16149Genomicunknown
ss2153150970USC_VALOUEV|NC_000008.10:g.11691142G>Tfwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat11/17/1611/17/16150Genomicunknown
ss2300645843HUMAN_LONGEVITY|HLI-8-11833633-G-Tfwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat11/18/1611/18/16150Genomicunknown
ss2470271552TOPMED|8_11691142_G/Tfwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat11/20/1611/20/16150Genomicunknown
ss2626949467SYSTEMSBIOZJU|SYSTEMSBIOZJU_SNV3465195fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat01/06/1701/06/17151Genomicunknown
ss2634708686ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_kgp12527549-0_B_F_18090894fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat02/02/1702/02/17151Genomicunknown
ss2708904582GRF|rs11250168fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat02/13/1702/13/17151Genomicunknown
ss2863168822GNOMAD|rs11250168fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat05/19/1705/19/17151Genomicunknown
ss2985431135AFFY|Axiom_PsorMich_Affx-31399951fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat05/24/1705/24/17151Genomicunknown
ss2986073087AFFY|Axiom_Smokesc1_Affx-31399951fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat05/24/1705/24/17151Genomicunknown
ss3002656656SWEGEN|NC_000008.10:g.11691142G>Tfwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat05/30/1705/30/17151Genomicunknown
ss3026253391BIOINF_KMB_FNS_UNIBA|8.11833633G>Tfwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat07/05/1707/05/17151Genomicunknown
ss3348035505CSHL|rs11250168fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat10/02/1710/02/17151Genomicunknown
ss3553739855TOPMED|TOPMed_freeze_5?chr8:11,833,633-01fwd/C/Gtgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat10/06/1710/06/17151Genomicunknown
ss3553739856TOPMED|TOPMed_freeze_5?chr8:11,833,633-02fwd/G/Ttgagggcgagggtgggcagtctacattggctgagccctgtttttgtgaat10/06/1710/06/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs11250168|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='C/G/T'|mol=Genomic|build=151
 TAGTCACTAG ATGAAAATAT TCAGCCAGTG ACCCAAAAAA TTGCTACCAA TGAGACTCTC
 CATTTTGCCA TGTAGCCAGA ACTTACTTTG ATCTATGTGC CTGGGGTAGT GACCAAGTAG
 GTGGGTAGGA GTAATCTCAG GGAAACTTGA GGCCCCAGCC TCATGGCTAG GGTCATAATT
 TGAACCCAGG TCTGTCTGAC ATCAGAATCC ATGATGTTAA CCCCAATTCT AAGGGGTTCA
 ACTACCCTTT CTAAATGGAA TCCTGCTATA TTAAGCACTA TTTATTCATT TTATATAAAC
 TAGAAACATT TTATGTAGTA AGTAGTTGAG AGTGTTTTGG TTTTGCAGTT TGATCACTAG
 TTTTAGAAAC CAGTTTTTAA ACACTTTGTG GCCAATTCCA TTACTATATT AAAATTCAGA
 TTTATTTGGT TTTTCCTTAA CTATTGGGAT TAAATCCTGG TTGTAATTCA TAGTTTGAGG
 GCGAGGGTGG GCAGTCTACA
 B
 TTGGCTGAGC CCTGTTTTTG TGAATAAATG TTATCAGAAC ACAGCCACAC CCATTTGCTT
 CTTTGTCTTC TGTGGCTGCT TTTGCAATGT GACGGCCGAG TTGAGGAGCT GCAACAGGCG
 ATGACTTGTA AAGCTGAAAA TATTTTTTGG CCCTTGAATA AGAGGTTTGC TGACTTCTGA
 CTTAGGGTAT CAGTTGTTCT GTTATCCCAG TAAAACTCAA GGCATTAGGG GAGAAATGTT
 AATATTAATA CTTAAGTTGA TTTGATTTAG GGAAATCTTT GAAGATTTCT AAGTCTTAAG
 CAGTAGAACC TGTTAATGGT TTTAGTTTCA GCAGTAAGGA CATTTTACAA GTAAAGTTTT
 AAATGAAAAC ATTTTGTATG AAGCCACAAG TCGTCTGGCC TCTTGCTGGT GTCCAGATAT
 TAACACTGAT CCTATTTCTC CTTGCTGACC AAGTCTGTCC TTTGTAGTAA GAAAGGAAGA
 AACGTTGACT CTGTCCGATC

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_077531 ABBA01026877
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.
SourceG/G
G/T
T/T
HWPG
T
ss1328577332EAS 1008AF 0.544600010.45540002
EUR 1006AF 0.813099980.18689999
AFR 1322AF 0.804099980.19589999
AMR 694AF 0.765099940.23490000
SAS 978AF 0.755600040.24439999
ss134552615ENSEMBL_Venter 2IG 1.00000000 0.500000000.50000000
ENSEMBL_celera 2IG 1.00000000 1.00000000
ss143253598ENSEMBL_Watson 2IG 1.00000000 0.500000000.50000000
ss163927789YRISub-Saharan African 2IG 1.00000000 0.500000000.50000000
ss166222400PGP 2IG 1.00000000 0.500000000.50000000
ss223535850pilot_1_YRI_low_coverage_panel 118AF 0.771186410.22881356
ss234315153pilot_1_CEU_low_coverage_panel 120AF 0.850000020.15000001
ss241197826pilot_1_CHB+JPT_low_coverage_panel 120AF 0.491666670.50833333
ss43287234HapMap-CEUEuropean 120IG0.783333360.183333340.033333340.250592000.875000000.12500000
HapMap-HCBAsian 84IG0.380952390.428571430.190476190.479500000.595238090.40476191
HapMap-JPTAsian 172IG0.337209310.465116290.197674420.654721000.569767420.43023255
HapMap-YRISub-Saharan African 224IG0.616071400.312500000.071428570.250592000.772321400.22767857
HAPMAP-ASW 98IG0.714285730.224489790.061224490.150222000.826530640.17346939
HAPMAP-CHBAsian 82IG0.268292700.536585390.195121940.654721000.536585390.46341464
HAPMAP-CHD 170IG0.294117660.529411790.176470590.527089000.558823530.44117647
HAPMAP-GIH 174IG0.586206910.356321840.057471261.000000000.764367820.23563218
HAPMAP-LWK 180IG0.733333350.244444440.022222221.000000000.855555530.14444445
HAPMAP-MEX 96IG0.500000000.416666660.083333341.000000000.708333310.29166666
HAPMAP-TSI 172IG0.593023240.313953490.093023260.150222000.750000000.25000000
ENSEMBL_Watson 2IG1.00000000 1.00000000
ss98049029J. Craig Venter 2IG 1.00000000 0.500000000.50000000

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
Additional Freq. Data
0.386+/-0.2100000ALFRED: 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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