rs7101429
A SNP in the GAB2 gene on chromosome 11. Its most notable genotype is G;G: 0.70x reduced risk for Alzheimer's risk
- Gene
- GAB2
- Location
- Chr 1178,281,921 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 23%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;ABadhigher Alzheimer's risk if ApoE4 also present
- A;GGood0.70x reduced risk for Alzheimer's risk
- G;GMost notableGood0.70x reduced risk for Alzheimer's risk
On SNPedia: (A;A), (A;G), (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 61% A;G 33% G;G 7%
- European ancestry (Utah)A;A 75% A;G 23% G;G 2%
- Han Chinese (Beijing)A;A 42% A;G 42% G;G 17%
- Japanese (Tokyo)A;A 26% A;G 51% G;G 23%
- Yoruba (Nigeria)A;A 95% A;G 5% G;G <1%
- African ancestry (Southwest US)A;A 91% A;G 9% G;G 0%
- Chinese (Denver)A;A 34% A;G 55% G;G 11%
- Gujarati IndianA;A 42% A;G 50% G;G 9%
- Luhya (Kenya)A;A 89% A;G 11% G;G 0%
- Mexican ancestry (Los Angeles)A;A 47% A;G 47% G;G 7%
- Maasai (Kenya)A;A 70% A;G 28% G;G 3%
- TuscanA;A 57% A;G 39% G;G 4%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs7101429 is a SNP in the GRB2-associated binding protein 2 GAB2 gene. In a study of 4000 DNA samples from ~1300 families affected by Alzheimer's disease, there was a reduced risk (0.70x; p = .002) among carriers of the rs7101429(G) minor allele.
Source and license
Adapted from rs7101429 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.