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rs121912579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121912579(A;T)
Make rs121912579(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position51078351
GeneSMAD4
is asnp
is mentioned by
dbSNPrs121912579
ebirs121912579
HLIrs121912579
Exacrs121912579
Varsomers121912579
Maprs121912579
PheGenIrs121912579
hapmaprs121912579
1000 genomesrs121912579
hgdprs121912579
ensemblrs121912579
gopubmedrs121912579
geneviewrs121912579
scholarrs121912579
googlers121912579
pharmgkbrs121912579
gwascentralrs121912579
openSNPrs121912579
23andMers121912579
23andMe allrs121912579
SNP Nexus

SNPshotrs121912579
SNPdbers121912579
MSV3drs121912579
GWAS Ctlgrs121912579
Max Magnitude0
OMIM600993
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121912579(T;T)
Alt rs121912579(T;T)
Reference rs121912579(A;A)
Significance Pathogenic
Disease Carcinoma of pancreas
Variation info
Gene SMAD4
CLNDBN Carcinoma of pancreas
Reversed 0
HGVS NC_000018.9:g.48604721A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009065.4,