rs1001179
A SNP in the CAT gene on chromosome 11. Its most notable genotype is T;T: 0.6x decreased acoustic neuroma risk
- Gene
- CAT
- Location
- Chr 1134,438,684 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 12%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableNot rated0.6x decreased acoustic neuroma risk
- C;TNot rated0.6x decreased acoustic neuroma risk
- C;CNot ratednormal
SNPedia records rs1001179 on the minus strand: (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.
- AverageT;T 2% C;T 16% C;C 82%
- European ancestry (Utah)T;T 4% C;T 41% C;C 56%
- Han Chinese (Beijing)T;T 0% C;T 6% C;C 94%
- Japanese (Tokyo)T;T 0% C;T 5% C;C 95%
- Yoruba (Nigeria)T;T 0% C;T 2% C;C 98%
- African ancestry (Southwest US)T;T 0% C;T 7% C;C 93%
- Chinese (Denver)T;T <1% C;T 7% C;C 92%
- Gujarati IndianT;T 2% C;T 35% C;C 63%
- Luhya (Kenya)T;T <1% C;T 5% C;C 95%
- Mexican ancestry (Los Angeles)T;T 7% C;T 26% C;C 67%
- Maasai (Kenya)T;T 0% C;T 12% C;C 89%
- TuscanT;T 5% C;T 32% C;C 63%
Notes
From SNPedia
Notes
A study of non-Hispanic Caucasians with various types of brain tumors concluded that there was an decreased risk of acoustic neuroma (odds ratio 0.6, CI: 0.3-1.0) associated with the rs1001179(A) allele, as oriented in dbSNP orientation (and not as published). {{PMID Auto |PMID=21795425 |Title=Genetic Variation in Myeloperoxidase Modifies the Association of Serum {alpha}-Tocopherol with Aggressive Prostate Cancer among Current Smokers |OA=1 }}
Source and license
Adapted from rs1001179 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.