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rs768713596

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768713596(C;T)
Make rs768713596(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67164965
GeneSMAD3
is asnp
is mentioned by
dbSNPrs768713596
ebirs768713596
HLIrs768713596
Exacrs768713596
Varsomers768713596
Maprs768713596
PheGenIrs768713596
hapmaprs768713596
1000 genomesrs768713596
hgdprs768713596
ensemblrs768713596
gopubmedrs768713596
geneviewrs768713596
scholarrs768713596
googlers768713596
pharmgkbrs768713596
gwascentralrs768713596
openSNPrs768713596
23andMers768713596
23andMe allrs768713596
SNP Nexus

SNPshotrs768713596
SNPdbers768713596
MSV3drs768713596
GWAS Ctlgrs768713596
Max Magnitude0
ClinVar
Risk rs768713596(T;T)
Alt rs768713596(T;T)
Reference rs768713596(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67457303C>T
CLNSRC
CLNACC RCV000196995.2,