rs121908677
A SNP in the SLC7A7 gene on chromosome 14. Its most notable genotype is A;C: Carrier of a lysinuric protein intolerance mutation
- Gene
- SLC7A7
- Location
- Chr 1422,813,238 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- Not on consumer chips
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- A;CMost notableBadCarrier of a lysinuric protein intolerance mutation
SNPedia records rs121908677 on the minus strand: (G;G), (G;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Notes
From SNPedia
Notes
aka c.161G>T (p.Gly54Val or G54V)
A;C
Unaffected in absence of a second SLC7A7 gene mutation
Source and license
Adapted from rs121908677 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.