rs77558292
A SNP in the RET gene on chromosome 10. Its most notable genotype is C;T: Multiple Endocrine Neoplasia IIA
- Gene
- RET
- Location
- Chr 1043,113,621 (GRCh38)
- Highest magnitude
- 5.1Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;TMost notableBadMultiple Endocrine Neoplasia IIA
- G;TBadMultiple Endocrine Neoplasia IIA
- T;TGoodcommon in clinvar
On SNPedia: (C;T), (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other RET SNPs
- rs74799832C;TMultiple Endocrine Neoplasia IIAVery important
- rs77316810A;TMultiple Endocrine Neoplasia IIAVery important
- rs77503355A;GMultiple 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
- rs79890926C;GMultiple Endocrine Neoplasia IIAVery important
Source and license
Adapted from rs77558292 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.