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rs201263330

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201263330(G;T)
Make rs201263330(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67190480
GeneSMAD3
is asnp
is mentioned by
dbSNPrs201263330
dbSNP (classic)rs201263330
ClinGenrs201263330
ebirs201263330
HLIrs201263330
Exacrs201263330
Gnomadrs201263330
Varsomers201263330
LitVarrs201263330
Maprs201263330
PheGenIrs201263330
Biobankrs201263330
1000 genomesrs201263330
hgdprs201263330
ensemblrs201263330
geneviewrs201263330
scholarrs201263330
googlers201263330
pharmgkbrs201263330
gwascentralrs201263330
openSNPrs201263330
23andMers201263330
SNPshotrs201263330
SNPdbers201263330
MSV3drs201263330
GWAS Ctlgrs201263330
Max Magnitude0
ClinVar
Risk rs201263330(C;C) rs201263330(T;T)
Alt rs201263330(C;C) rs201263330(T;T)
Reference Rs201263330(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67482818G>C
CLNSRC
CLNACC RCV000198134.2,