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rs121912578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912578(C;C)
Make rs121912578(C;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position51078285
GeneSMAD4
is asnp
is mentioned by
dbSNPrs121912578
ebirs121912578
HLIrs121912578
Exacrs121912578
Varsomers121912578
Maprs121912578
PheGenIrs121912578
hapmaprs121912578
1000 genomesrs121912578
hgdprs121912578
ensemblrs121912578
gopubmedrs121912578
geneviewrs121912578
scholarrs121912578
googlers121912578
pharmgkbrs121912578
gwascentralrs121912578
openSNPrs121912578
23andMers121912578
23andMe allrs121912578
SNP Nexus

SNPshotrs121912578
SNPdbers121912578
MSV3drs121912578
GWAS Ctlgrs121912578
Merged fromRs28936392
Max Magnitude0
OMIM600993
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121912578(C;C)
Alt rs121912578(C;C)
Reference rs121912578(G;G)
Significance Pathogenic
Disease Carcinoma of pancreas
Variation info
Gene SMAD4
CLNDBN Carcinoma of pancreas
Reversed 0
HGVS NC_000018.9:g.48604655G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009064.4,