rs202085145
A SNP in the SUOX gene on chromosome 12. Its most notable genotype is T;T: Sulfite oxidase deficiency (predicted)
- Gene
- SUOX
- Location
- Chr 1256,002,720 (GRCh38)
- Highest magnitude
- 8.0Very important
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GGoodcommon/normal
- G;TBadCarrier of sulfite oxidase deficiency mutation; possible effects?
- T;TMost notableBadSulfite oxidase deficiency (predicted)
On SNPedia: (G;G), (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
aka c.228G>T, p.Arg76Ser, R76S ClinVar indicated "uncertain significance" for sulfite oxidase deficiency, also known as Sulfocysteinuria, listed in OMIM as a recessively inherited condition; in , this variant appears to have some effect even if inherited in only one copy (see paper for discussion).
G;T
Presumably unaffected in absence of a second SUOX gene mutation, however, see potential effects discussed in article cited in text on main rs-page.
T;T
see discussion and links via main rs-page
Source and license
Adapted from rs202085145 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.