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rs863223414

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223414(A;A)
Make rs863223414(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51913237
GeneACVRL1
is asnp
is mentioned by
dbSNPrs863223414
ebirs863223414
HLIrs863223414
Exacrs863223414
Varsomers863223414
Maprs863223414
PheGenIrs863223414
hapmaprs863223414
1000 genomesrs863223414
hgdprs863223414
ensemblrs863223414
gopubmedrs863223414
geneviewrs863223414
scholarrs863223414
googlers863223414
pharmgkbrs863223414
gwascentralrs863223414
openSNPrs863223414
23andMers863223414
23andMe allrs863223414
SNP Nexus

SNPshotrs863223414
SNPdbers863223414
MSV3drs863223414
GWAS Ctlgrs863223414
Max Magnitude0
ClinVar
Risk rs863223414(A;A)
Alt rs863223414(A;A)
Reference rs863223414(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACVRL1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52307021G>A
CLNSRC
CLNACC RCV000200439.1,