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rs863223771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223771(-;-)
Make rs863223771(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67165335
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223771
dbSNP (classic)rs863223771
ClinGenrs863223771
ebirs863223771
HLIrs863223771
Exacrs863223771
Gnomadrs863223771
Varsomers863223771
LitVarrs863223771
Maprs863223771
PheGenIrs863223771
Biobankrs863223771
1000 genomesrs863223771
hgdprs863223771
ensemblrs863223771
geneviewrs863223771
scholarrs863223771
googlers863223771
pharmgkbrs863223771
gwascentralrs863223771
openSNPrs863223771
23andMers863223771
SNPshotrs863223771
SNPdbers863223771
MSV3drs863223771
GWAS Ctlgrs863223771
Max Magnitude0
ClinVar
Risk rs863223771(-;-)
Alt rs863223771(-;-)
Reference Rs863223771(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67457673delC
CLNSRC
CLNACC RCV000199186.1,