rs387906588
A SNP in the ACVR1 gene on chromosome 2. Its most notable genotype is A;C: Fibrodysplasia ossificans progressiva
- Gene
- ACVR1
- Location
- Chr 2157,766,005 (GRCh38)
- Highest magnitude
- 7.0Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- A;CMost notableBadFibrodysplasia ossificans progressiva
SNPedia records rs387906588 on the minus strand: (G;G), (G;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other ACVR1 SNPs
- rs121912678C;TFibrodysplasia ossificans progressivaVery important
- rs121912679C;TFibrodysplasia ossificans progressivaVery important
- rs121912680C;GFibrodysplasia ossificans progressivaVery important
- rs387906589C;TFibrodysplasia ossificans progressivaVery important
- rs387906590C;GFibrodysplasia ossificans progressivaVery important
- rs387906591A;CFibrodysplasia ossificans progressivaVery important
- rs797045135A;GFibrodysplasia ossificans progressivaVery important
- rs1146031T;Tcommon genotypeTypical
Notes
From SNPedia
Notes
A;C
see Fibrodysplasia ossificans progressiva
Source and license
Adapted from rs387906588 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.