rs150681845
A SNP in the INTU gene on chromosome 4. Its most notable genotype is A;A: Orofaciodigital syndrome likely
- Gene
- INTU
- Location
- Chr 4127,687,772 (GRCh38)
- Highest magnitude
- 9.0Very important
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadOrofaciodigital syndrome likely
- A;GBadCarrier of an orofaciodigital mutation
- G;GGoodcommon/normal
On SNPedia: (A;A), (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
see
Source and license
Adapted from rs150681845 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.