rs2075912
A SNP in the RET gene on chromosome 10. Its most notable genotype is T;T: common in clinvar
- Gene
- RET
- Location
- Chr 1043,126,769 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 24%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageT;T 9%
- European ancestry (Utah)T;T 2%
- Han Chinese (Beijing)T;T 29%
- Japanese (Tokyo)T;T 30%
- Yoruba (Nigeria)T;T 0%
- African ancestry (Southwest US)T;T 0%
- Chinese (Denver)T;T 28%
- Gujarati IndianT;T 7%
- Luhya (Kenya)T;T 0%
- Mexican ancestry (Los Angeles)T;T 2%
- Maasai (Kenya)T;T 2%
- TuscanT;T 5%
Related
Other RET SNPs
- rs74799832C;TMultiple Endocrine Neoplasia IIAVery important
- rs77316810A;TMultiple Endocrine Neoplasia IIAVery important
- rs77503355A;GMultiple Endocrine Neoplasia IIAVery important
- rs77558292C;TMultiple Endocrine Neoplasia IIAVery important
- rs77709286C;GMultiple Endocrine Neoplasia IIAVery important
- rs78935588C;GMultiple Endocrine Neoplasia IIAVery important
- rs79658334C;GMultiple Endocrine Neoplasia IIAVery important
- rs79781594A;GMultiple Endocrine Neoplasia IIAVery important
Source and license
Adapted from rs2075912 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.