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rs863223412

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223412(A;A)
Make rs863223412(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51915438
GeneACVRL1
is asnp
is mentioned by
dbSNPrs863223412
ebirs863223412
HLIrs863223412
Exacrs863223412
Varsomers863223412
Maprs863223412
PheGenIrs863223412
hapmaprs863223412
1000 genomesrs863223412
hgdprs863223412
ensemblrs863223412
gopubmedrs863223412
geneviewrs863223412
scholarrs863223412
googlers863223412
pharmgkbrs863223412
gwascentralrs863223412
openSNPrs863223412
23andMers863223412
23andMe allrs863223412
SNP Nexus

SNPshotrs863223412
SNPdbers863223412
MSV3drs863223412
GWAS Ctlgrs863223412
Max Magnitude0
ClinVar
Risk rs863223412(A;A)
Alt rs863223412(A;A)
Reference rs863223412(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACVRL1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52309222G>A
CLNSRC
CLNACC RCV000197384.1,