rs863224484
A SNP in the PTCH1 gene on chromosome 9. Its most notable genotype is -;C: Possible miscall in 23andMe and Ancestry data; otherwise, Basal cell nevus syndrome
- Gene
- PTCH1
- Location
- Chr 995,459,688 (GRCh38)
- Highest magnitude
- 5.3Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- -;CMost notableBadPossible miscall in 23andMe and Ancestry data; otherwise, Basal cell nevus syndrome
- C;CGoodcommon in clinvar
SNPedia records rs863224484 on the minus strand: (-;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other PTCH1 SNPs
- rs199476090A;GBasal cell nevus syndromeVery important
- rs766313615A;GBasal cell nevus syndromeVery important
- rs778260156G;TBasal cell nevus syndromeVery important
- rs786204056A;GBasal cell nevus syndromeVery important
- rs863224442C;TBasal cell nevus syndromeVery important
- rs863224443C;TBasal cell nevus syndromeVery important
- rs863224444C;TBasal cell nevus syndromeVery important
- rs863224485-;TGGGTCCABasal cell nevus syndromeVery important
Notes
From SNPedia
Notes
aka c.2601delG (and due to alternative numbering, also c.2346delG, c.2601delG, c.2643delG, c.2796delG, and c.2799delG)
Source and license
Adapted from rs863224484 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.