rs121908641
A SNP in the ASS1 gene on chromosome 9. Its most notable genotype is A;G: Carrier of a citrullinemia type I mutation
- Gene
- ASS1
- Location
- Chr 9130,499,545 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadCarrier of a citrullinemia type I mutation
- G;GGoodcommon in clinvar
On SNPedia: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
aka c.1168G>A (p.Gly390Arg Or G390R)
A;G
Unaffected in absence of a second ASS1 gene mutation
Source and license
Adapted from rs121908641 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.