rs387907246
A SNP in the KCTD7 gene on chromosome 7. Its most notable genotype is C;T: Carrier of progressive myoclonus epilepsy allele
- Gene
- KCTD7
- Location
- Chr 766,638,912 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- C;TMost notableBadCarrier of progressive myoclonus epilepsy allele
On SNPedia: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other KCTD7 SNPs
- rs141191660A;GCarrier of progressive myoclonus epilepsy alleleImportant
- rs267607199C;TCarrier of progressive myoclonus epilepsy alleleImportant
- rs387907260C;TCarrier of progressive myoclonus epilepsy alleleImportant
- rs387907261A;TCarrier of progressive myoclonus epilepsy alleleImportant
- rs387907263A;CCarrier of progressive myoclonus epilepsy alleleImportant
- rs727502785-;CCarrier of progressive myoclonus epilepsy alleleImportant
Notes
From SNPedia
Notes
C;T
see discussion at KCTD7
Source and license
Adapted from rs387907246 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.