rs363717
A SNP in the ABCA1 gene on chromosome 9. Its most notable genotype is C;C: common in clinvar
- Gene
- ABCA1
- Location
- Chr 9104,782,419 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 15%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs363717 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageC;C 1%
- European ancestry (Utah)C;C 2%
- Han Chinese (Beijing)C;C 4%
- Japanese (Tokyo)C;C 3%
- Yoruba (Nigeria)C;C 0%
- African ancestry (Southwest US)C;C 0%
- Chinese (Denver)C;C 3%
- Gujarati IndianC;C 0%
- Luhya (Kenya)C;C 0%
- Mexican ancestry (Los Angeles)C;C 0%
- Maasai (Kenya)C;C 0%
- TuscanC;C 4%
Related
Other ABCA1 SNPs
- rs4149268C;Tassociated with higher HDL cholesterolWorth knowing
- rs4149274G;GAssociated with higher HDL (good) cholesterol.Minor
- rs2066714T;Tcommon in clinvarTypical
- rs2066715C;Ccommon in complete genomicsTypical
- rs2230808T;Tcommon in clinvarTypical
- rs2297404G;GNo summary available.Typical
- rs2515629A;Acommon in complete genomicsTypical
- rs2853579G;Gcommon in clinvarTypical
Notes
From SNPedia
Notes
Examining the effect of linkage disequilibrium between markers on the Type I error rate and power of nonparametric multipoint linkage analysis of two-generation and multigenerational pedigrees in the presence of missing genotype data. A survey of ABCA1 sequence variation confirms association with dementia.
Source and license
Adapted from rs363717 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.