rs200322968
A SNP in the WDPCP gene on chromosome 2. Its most notable genotype is T;T: Orofaciodigital syndrome likely
- Gene
- WDPCP
- Location
- Chr 263,492,856 (GRCh38)
- Highest magnitude
- 9.0Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- C;TBadCarrier of an orofaciodigital mutation
- T;TMost notableBadOrofaciodigital syndrome likely
On SNPedia: (C;C), (C;T), (T;T). 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 rs200322968 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.