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rs863223406

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223406(A;A)
Make rs863223406(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51919116
GeneACVRL1
is asnp
is mentioned by
dbSNPrs863223406
ebirs863223406
HLIrs863223406
Exacrs863223406
Varsomers863223406
Maprs863223406
PheGenIrs863223406
hapmaprs863223406
1000 genomesrs863223406
hgdprs863223406
ensemblrs863223406
gopubmedrs863223406
geneviewrs863223406
scholarrs863223406
googlers863223406
pharmgkbrs863223406
gwascentralrs863223406
openSNPrs863223406
23andMers863223406
23andMe allrs863223406
SNP Nexus

SNPshotrs863223406
SNPdbers863223406
MSV3drs863223406
GWAS Ctlgrs863223406
Max Magnitude0
ClinVar
Risk rs863223406(A;A)
Alt rs863223406(A;A)
Reference rs863223406(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACVRL1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52312900G>A
CLNSRC
CLNACC RCV000197808.1,