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rs863223407

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223407(A;A)
Make rs863223407(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51920796
GeneACVRL1
is asnp
is mentioned by
dbSNPrs863223407
ebirs863223407
HLIrs863223407
Exacrs863223407
Varsomers863223407
Maprs863223407
PheGenIrs863223407
hapmaprs863223407
1000 genomesrs863223407
hgdprs863223407
ensemblrs863223407
gopubmedrs863223407
geneviewrs863223407
scholarrs863223407
googlers863223407
pharmgkbrs863223407
gwascentralrs863223407
openSNPrs863223407
23andMers863223407
23andMe allrs863223407
SNP Nexus

SNPshotrs863223407
SNPdbers863223407
MSV3drs863223407
GWAS Ctlgrs863223407
Max Magnitude0
ClinVar
Risk rs863223407(A;A)
Alt rs863223407(A;A)
Reference rs863223407(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACVRL1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52314580G>A
CLNSRC
CLNACC RCV000199656.1,