rs72658154
A SNP in the COL1A2 gene on chromosome 7. Its most notable genotype is A;G: Osteogenesis imperfecta type II
- Gene
- COL1A2
- Location
- Chr 794,418,518 (GRCh38)
- Highest magnitude
- 7.7Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadOsteogenesis imperfecta type II
- 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
Notes
From SNPedia
Notes
aka c.1991G>A (p.Gly664Asp) 23andMe name: i5041058
A;G
see links via main rs-page
Source and license
Adapted from rs72658154 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.