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rs863223742

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223742(C;C)
Make rs863223742(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67184726
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223742
ebirs863223742
HLIrs863223742
Exacrs863223742
Varsomers863223742
Maprs863223742
PheGenIrs863223742
hapmaprs863223742
1000 genomesrs863223742
hgdprs863223742
ensemblrs863223742
gopubmedrs863223742
geneviewrs863223742
scholarrs863223742
googlers863223742
pharmgkbrs863223742
gwascentralrs863223742
openSNPrs863223742
23andMers863223742
23andMe allrs863223742
SNP Nexus

SNPshotrs863223742
SNPdbers863223742
MSV3drs863223742
GWAS Ctlgrs863223742
Max Magnitude0
ClinVar
Risk rs863223742(C;C)
Alt rs863223742(C;C)
Reference rs863223742(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67477064G>C
CLNSRC
CLNACC RCV000200134.1,