rs267606795
A SNP in the FAM20C gene on chromosome 7. Its most notable genotype is C;C: Raine syndrome
- Gene
- FAM20C
- Location
- Chr 7255,869 (GRCh38)
- Highest magnitude
- 9.0Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableBadRaine syndrome
- C;GBadunaffected carrier of Raine syndrome allele
- G;GGoodcommon in clinvar
On SNPedia: (C;C), (C;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Notes
From SNPedia
Notes
C;C
Unless there has been a data mix-up (which is always possible for C/G SNPs prone to ambiguous flips), this genotype represents a patient with two copies of a defective allele associated with Raine syndrome, also known as osteosclerotic bone dysplasia.
Source and license
Adapted from rs267606795 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.