rs121917758
A SNP in the LRRC56 gene on chromosome 11. Its most notable genotype is A;G: Costello syndrome
- Gene
- LRRC56
- Location
- Chr 11533,883 (GRCh38)
- Highest magnitude
- 7.0Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- A;GMost notableBadCostello syndrome
SNPedia records rs121917758 on the minus strand: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
aka c.173C>T (p.Thr58Ile) 23andMe name: i5005668
A;G
See links via main rs-page
Source and license
Adapted from rs121917758 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.