rs924607
A SNP in the LOC100996325 gene on chromosome 5. Its most notable genotype is T;T: in childhood acute lymphoblastic leukemia patients, worse response to vincristine
- Gene
- LOC100996325
- Location
- Chr 5609,978 (GRCh38)
- Highest magnitude
- 1.5Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon/normal
- C;TGoodcommon/normal
- T;TMost notableBadin childhood acute lymphoblastic leukemia patients, worse response to vincristine
On SNPedia: (C;C), (C;T), (T;T). 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 58% C;T 33% T;T 9%
- European ancestry (Utah)C;C 39% C;T 44% T;T 17%
- Han Chinese (Beijing)C;C 31% C;T 53% T;T 17%
- Japanese (Tokyo)C;C 53% C;T 36% T;T 11%
- Yoruba (Nigeria)C;C 83% C;T 16% T;T <1%
- African ancestry (Southwest US)C;C 81% C;T 18% T;T 2%
- Chinese (Denver)C;C 53% C;T 39% T;T 8%
- Gujarati IndianC;C 42% C;T 47% T;T 12%
- Luhya (Kenya)C;C 91% C;T 9% T;T 0%
- Mexican ancestry (Los Angeles)C;C 55% C;T 36% T;T 9%
- Maasai (Kenya)C;C 82% C;T 17% T;T <1%
- TuscanC;C 28% C;T 49% T;T 24%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
In a study of ~300 patients with childhood acute lymphoblastic leukemia (ALL) treated with vincristine, rs924607(T;T) patients, 28 of 50 (56%) developed at least 1 episode of grade 2 to 4 peripheral neuropathy. This was a significantly higher rate than in patients with (C;C) or (C;T) genotypes (58/271 patients; p = 2.4×10e-6). The severity of neuropathy was also greater in (T;T) patients.
T;T
(T;T) pediatric ALL patients being treated with vincristine have twice the risk of developing peripheral neuropathies compared to (C;C) and (C;T) patients, based on a preliminary study of ~300 patients.
Source and license
Adapted from rs924607 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.