rs7577363
A SNP in the ALK gene on chromosome 2. Its most notable genotype is A;A: >1.37x risk
- Gene
- ALK
- Location
- Chr 229,653,477 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 8%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot rated>1.37x risk
- A;GNot rated1.37x risk
- C;CNot ratedNo summary available.
- G;GGoodcommon
On SNPedia: (A;A), (A;G), (C;C), (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.
- AverageA;A 2% A;G 16% C;C 0% G;G 82%
- European ancestry (Utah)A;A 0% A;G 6% C;C 0% G;G 94%
- Han Chinese (Beijing)A;A 0% A;G 0% C;C 0% G;G 100%
- Japanese (Tokyo)A;A 0% A;G 0% C;C 0% G;G 100%
- Yoruba (Nigeria)A;A 8% A;G 37% C;C 0% G;G 56%
- African ancestry (Southwest US)A;A 2% A;G 21% C;C 0% G;G 77%
- Chinese (Denver)A;A 0% A;G <1% C;C 0% G;G 99%
- Gujarati IndianA;A 2% A;G 13% C;C 0% G;G 85%
- Luhya (Kenya)A;A 6% A;G 48% C;C 0% G;G 46%
- Mexican ancestry (Los Angeles)A;A 0% A;G 2% C;C 0% G;G 98%
- Maasai (Kenya)A;A 8% A;G 33% C;C 0% G;G 58%
- TuscanA;A 0% A;G 11% C;C 0% G;G 89%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs7577363 has been reported in a large study to be associated with multiple sclerosis. The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with this allele is 1.37 (CI 1.17-1.61).
Source and license
Adapted from rs7577363 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.