rs121912699
A SNP in the ACY1 gene on chromosome 3. Its most notable genotype is A;C: Carrier of an aminoacylase-1 deficiency mutation
- Gene
- ACY1
- Location
- Chr 351,987,188 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodcommon in clinvar
- A;CMost notableBadCarrier of an aminoacylase-1 deficiency mutation
On SNPedia: (A;A), (A;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Notes
From SNPedia
Notes
A;C
Unaffected in absence of a second mutation in the ACY1 gene; see links via main rs-page.
Source and license
Adapted from rs121912699 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.