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rs863223417

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223417(-;GT)
Make rs863223417(GT;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51915484
GeneACVRL1
is asnp
is mentioned by
dbSNPrs863223417
ClinGenrs863223417
ebirs863223417
HLIrs863223417
Exacrs863223417
Varsomers863223417
Maprs863223417
PheGenIrs863223417
hapmaprs863223417
1000 genomesrs863223417
hgdprs863223417
ensemblrs863223417
gopubmedrs863223417
geneviewrs863223417
scholarrs863223417
googlers863223417
pharmgkbrs863223417
gwascentralrs863223417
openSNPrs863223417
23andMers863223417
23andMe allrs863223417
SNP Nexus

SNPshotrs863223417
SNPdbers863223417
MSV3drs863223417
GWAS Ctlgrs863223417
Max Magnitude0
ClinVar
Risk rs863223417(GT;GT)
Alt rs863223417(GT;GT)
Reference Rs863223417(;)
Significance Pathogenic
Disease not provided
Variation info
Gene ACVRL1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52309267_52309268dupGT
CLNSRC
CLNACC RCV000199151.2,