rs28935482
A SNP in the NR0B1 gene on chromosome X. Its most notable genotype is G;G.
- Gene
- NR0B1
- Location
- Chr X30,308,491 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GMost notableNot ratedNo summary available.
- C;CGoodcommon in clinvar
SNPedia records rs28935482 on the minus strand: (C;C), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Notes
From SNPedia
Notes
G;G
probably the higher risk variant
Source and license
Adapted from rs28935482 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.