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rs794727798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727798(C;T)
Make rs794727798(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position67181384
GeneSMAD3
is asnp
is mentioned by
dbSNPrs794727798
dbSNP (classic)rs794727798
ClinGenrs794727798
ebirs794727798
HLIrs794727798
Exacrs794727798
Gnomadrs794727798
Varsomers794727798
LitVarrs794727798
Maprs794727798
PheGenIrs794727798
Biobankrs794727798
1000 genomesrs794727798
hgdprs794727798
ensemblrs794727798
geneviewrs794727798
scholarrs794727798
googlers794727798
pharmgkbrs794727798
gwascentralrs794727798
openSNPrs794727798
23andMers794727798
SNPshotrs794727798
SNPdbers794727798
MSV3drs794727798
GWAS Ctlgrs794727798
Max Magnitude0
ClinVar
Risk rs794727798(T;T)
Alt rs794727798(T;T)
Reference Rs794727798(C;C)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene SMAD3
CLNDBN not provided not specified
Reversed 0
HGVS NC_000015.9:g.67473722C>T
CLNSRC
CLNACC RCV000179456.4, RCV000235212.1,