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rs863223408

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223408(A;A)
Make rs863223408(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51920832
GeneACVRL1
is asnp
is mentioned by
dbSNPrs863223408
ebirs863223408
HLIrs863223408
Exacrs863223408
Varsomers863223408
Maprs863223408
PheGenIrs863223408
hapmaprs863223408
1000 genomesrs863223408
hgdprs863223408
ensemblrs863223408
gopubmedrs863223408
geneviewrs863223408
scholarrs863223408
googlers863223408
pharmgkbrs863223408
gwascentralrs863223408
openSNPrs863223408
23andMers863223408
23andMe allrs863223408
SNP Nexus

SNPshotrs863223408
SNPdbers863223408
MSV3drs863223408
GWAS Ctlgrs863223408
Max Magnitude0
ClinVar
Risk rs863223408(A;A)
Alt rs863223408(A;A)
Reference rs863223408(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACVRL1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52314616G>A
CLNSRC
CLNACC RCV000198604.1,