rs74315397
A SNP in the MKKS gene on chromosome 20. Its most notable genotype is A;T: Carrier of a Bardet-Biedl syndrome mutation
- Gene
- MKKS
- Location
- Chr 2010,412,723 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- A;TMost notableBadCarrier of a Bardet-Biedl syndrome mutation
- A;AGoodcommon in clinvar
SNPedia records rs74315397 on the minus strand: (A;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Notes
From SNPedia
Notes
A;T
Unaffected in absence of a second MKKS gene mutation
Source and license
Adapted from rs74315397 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.