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rs863224846

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224846(A;G)
Make rs863224846(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position157770386
GeneACVR1
is asnp
is mentioned by
dbSNPrs863224846
ebirs863224846
HLIrs863224846
Exacrs863224846
Varsomers863224846
Maprs863224846
PheGenIrs863224846
hapmaprs863224846
1000 genomesrs863224846
hgdprs863224846
ensemblrs863224846
gopubmedrs863224846
geneviewrs863224846
scholarrs863224846
googlers863224846
pharmgkbrs863224846
gwascentralrs863224846
openSNPrs863224846
23andMers863224846
23andMe allrs863224846
SNP Nexus

SNPshotrs863224846
SNPdbers863224846
MSV3drs863224846
GWAS Ctlgrs863224846
Max Magnitude0
ClinVar
Risk rs863224846(G;G)
Alt rs863224846(G;G)
Reference rs863224846(A;A)
Significance Probable-Pathogenic
Disease Progressive myositis ossificans
Variation info
Gene ACVR1
CLNDBN Progressive myositis ossificans
Reversed 1
HGVS NC_000002.11:g.158626898T>C
CLNSRC
CLNACC RCV000198218.1,