rs863224453
A SNP in the EPCAM gene on chromosome 2. Its most notable genotype is A;G: Lynch syndrome mutation
- Gene
- EPCAM
- Location
- Chr 247,385,165 (GRCh38)
- Highest magnitude
- 6.0Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadLynch syndrome mutation
- G;GGoodcommon in clinvar
On SNPedia: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other EPCAM SNPs
- rs376155665A;GLynch syndrome mutationVery important
- rs878854485C;TLynch syndrome mutationVery important
- rs878854491C;TLynch syndrome mutationVery important
- rs878854496A;GLynch syndrome mutationVery important
- rs267606785A;GCarrier of an infancy diarrhea mutationImportant
- rs397514661C;TCarrier of an infancy diarrhea mutationImportant
- rs606231203A;GCarrier of an infancy diarrhea mutationImportant
- rs606231204-;CCarrier of an infancy diarrhea mutationImportant
Source and license
Adapted from rs863224453 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.