rs797045135
A SNP in the ACVR1 gene on chromosome 2. Its most notable genotype is A;G: Fibrodysplasia ossificans progressiva
- Gene
- ACVR1
- Location
- Chr 2157,774,144 (GRCh38)
- Highest magnitude
- 7.0Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- A;GMost notableBadFibrodysplasia ossificans progressiva
- A;AGoodcommon in clinvar
SNPedia records rs797045135 on the minus strand: (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other ACVR1 SNPs
- rs121912678C;TFibrodysplasia ossificans progressivaVery important
- rs121912679C;TFibrodysplasia ossificans progressivaVery important
- rs121912680C;GFibrodysplasia ossificans progressivaVery important
- rs387906588A;CFibrodysplasia ossificans progressivaVery important
- rs387906589C;TFibrodysplasia ossificans progressivaVery important
- rs387906590C;GFibrodysplasia ossificans progressivaVery important
- rs387906591A;CFibrodysplasia ossificans progressivaVery important
- rs1146031T;Tcommon genotypeTypical
Source and license
Adapted from rs797045135 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.