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rs863223411

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223411(A;A)
Make rs863223411(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51915372
GeneACVRL1
is asnp
is mentioned by
dbSNPrs863223411
ebirs863223411
HLIrs863223411
Exacrs863223411
Varsomers863223411
Maprs863223411
PheGenIrs863223411
hapmaprs863223411
1000 genomesrs863223411
hgdprs863223411
ensemblrs863223411
gopubmedrs863223411
geneviewrs863223411
scholarrs863223411
googlers863223411
pharmgkbrs863223411
gwascentralrs863223411
openSNPrs863223411
23andMers863223411
23andMe allrs863223411
SNP Nexus

SNPshotrs863223411
SNPdbers863223411
MSV3drs863223411
GWAS Ctlgrs863223411
Max Magnitude0
ClinVar
Risk rs863223411(A;A)
Alt rs863223411(A;A)
Reference rs863223411(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACVRL1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52309156C>A
CLNSRC
CLNACC RCV000200622.1,