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rs121912576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912576(G;T)
Make rs121912576(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position51065539
GeneSMAD4
is asnp
is mentioned by
dbSNPrs121912576
ebirs121912576
HLIrs121912576
Exacrs121912576
Varsomers121912576
Maprs121912576
PheGenIrs121912576
hapmaprs121912576
1000 genomesrs121912576
hgdprs121912576
ensemblrs121912576
gopubmedrs121912576
geneviewrs121912576
scholarrs121912576
googlers121912576
pharmgkbrs121912576
gwascentralrs121912576
openSNPrs121912576
23andMers121912576
23andMe allrs121912576
SNP Nexus

SNPshotrs121912576
SNPdbers121912576
MSV3drs121912576
GWAS Ctlgrs121912576
Max Magnitude0
OMIM600993
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121912576(T;T)
Alt rs121912576(T;T)
Reference rs121912576(G;G)
Significance Pathogenic
Disease Carcinoma of pancreas
Variation info
Gene SMAD4
CLNDBN Carcinoma of pancreas
Reversed 0
HGVS NC_000018.9:g.48591909G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009062.4,