rs7762619
A SNP in the LOC100287329 gene on chromosome 6. Its most notable genotype is T;T: common in complete genomics
- Gene
- LOC100287329
- Location
- Chr 631,563,533 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 1%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 10 HapMap populations.
- AverageT;T 96%
- European ancestry (Utah)T;T 99%
- Han Chinese (Beijing)T;T 100%
- Japanese (Tokyo)T;T 100%
- Yoruba (Nigeria)T;T 99%
- African ancestry (Southwest US)T;T 97%
- Chinese (Denver)T;T 99%
- Luhya (Kenya)T;T 96%
- Mexican ancestry (Los Angeles)T;T 90%
- Maasai (Kenya)T;T 89%
- TuscanT;T 94%
Related
Other LOC100287329 SNPs
- rs1041981A;AHigher myocardial infarction riskWorth knowing
- rs1799724C;Tif ApoE4(-), 1.6x risk of AD; if (+), 6.6x riskWorth knowing
- rs1800630A;A1.8x increased lupus riskTypical
- rs2230365C;Ccommon in complete genomicsTypical
- rs2857708C;Ccommon in complete genomicsTypical
- rs3130062T;Tcommon on affy axiom dataTypical
Source and license
Adapted from rs7762619 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.