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rs121912577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912577(C;G)
Make rs121912577(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position51067115
GeneSMAD4
is asnp
is mentioned by
dbSNPrs121912577
ebirs121912577
HLIrs121912577
Exacrs121912577
Varsomers121912577
Maprs121912577
PheGenIrs121912577
hapmaprs121912577
1000 genomesrs121912577
hgdprs121912577
ensemblrs121912577
gopubmedrs121912577
geneviewrs121912577
scholarrs121912577
googlers121912577
pharmgkbrs121912577
gwascentralrs121912577
openSNPrs121912577
23andMers121912577
23andMe allrs121912577
SNP Nexus

SNPshotrs121912577
SNPdbers121912577
MSV3drs121912577
GWAS Ctlgrs121912577
Max Magnitude0
OMIM600993
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912577(G;G)
Alt rs121912577(G;G)
Reference rs121912577(C;C)
Significance Pathogenic
Disease Carcinoma of pancreas Juvenile polyposis syndrome
Variation info
Gene SMAD4
CLNDBN Carcinoma of pancreas Juvenile polyposis syndrome
Reversed 0
HGVS NC_000018.9:g.48593485C>G
CLNSRC ARUP SMAD4 OMIM Allelic Variant
CLNACC RCV000009063.4, RCV000021726.1,