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rs863223738

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223738(C;C)
Make rs863223738(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67181354
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223738
ebirs863223738
HLIrs863223738
Exacrs863223738
Varsomers863223738
Maprs863223738
PheGenIrs863223738
hapmaprs863223738
1000 genomesrs863223738
hgdprs863223738
ensemblrs863223738
gopubmedrs863223738
geneviewrs863223738
scholarrs863223738
googlers863223738
pharmgkbrs863223738
gwascentralrs863223738
openSNPrs863223738
23andMers863223738
23andMe allrs863223738
SNP Nexus

SNPshotrs863223738
SNPdbers863223738
MSV3drs863223738
GWAS Ctlgrs863223738
Max Magnitude0
ClinVar
Risk rs863223738(C;C)
Alt rs863223738(C;C)
Reference rs863223738(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67473692G>C
CLNSRC
CLNACC RCV000200741.1,