rs3740071
A SNP in the ABCC2 gene on chromosome 10. Its most notable genotype is G;G: common genotype
- Gene
- ABCC2
- Location
- Chr 1099,830,363 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3740071 on the minus strand: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageG;G 100%
- European ancestry (Utah)G;G 100%
- Han Chinese (Beijing)G;G 100%
- Japanese (Tokyo)G;G 100%
- Yoruba (Nigeria)G;G 100%
Related
Other ABCC2 SNPs
- rs2273697A;AAdverse reaction more likely to carbamazepine in epileptic patientsMinor
- rs717620C;Ccommon in clinvarTypical
- rs927344T;Tcommon in complete genomicsTypical
- rs3740066T;T4.4x risk for ICPTypical
- rs8187710G;Gcommon on affy axiom dataTypical
- rs17222547C;Ccommon in clinvarTypical
- rs17222723T;Tcommon on affy axiom dataTypical
Source and license
Adapted from rs3740071 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.