rs17857727
A SNP in the RET gene on chromosome 10. Its most notable genotype is G;G.
- Gene
- RET
- Location
- Chr 1043,100,520 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageG;G 59%
- European ancestry (Utah)G;G 48%
- Han Chinese (Beijing)G;G 23%
- Japanese (Tokyo)G;G 30%
- Yoruba (Nigeria)G;G 96%
- African ancestry (Southwest US)G;G 88%
- Chinese (Denver)G;G 28%
- Gujarati IndianG;G 45%
- Luhya (Kenya)G;G 93%
- Mexican ancestry (Los Angeles)G;G 74%
- Maasai (Kenya)G;G 64%
- TuscanG;G 59%
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 rs17857727 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.