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rs1057519962

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519962(A;A)
Make rs1057519962(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position51067035
GeneSMAD4
is asnp
is mentioned by
dbSNPrs1057519962
dbSNP (old)rs1057519962
ClinGenrs1057519962
ebirs1057519962
HLIrs1057519962
Exacrs1057519962
Gnomadrs1057519962
Varsomers1057519962
LitVarrs1057519962
Maprs1057519962
PheGenIrs1057519962
Biobankrs1057519962
1000 genomesrs1057519962
hgdprs1057519962
ensemblrs1057519962
gopubmedrs1057519962
geneviewrs1057519962
scholarrs1057519962
googlers1057519962
pharmgkbrs1057519962
gwascentralrs1057519962
openSNPrs1057519962
23andMers1057519962
23andMe allrs1057519962
SNPshotrs1057519962
SNPdbers1057519962
MSV3drs1057519962
GWAS Ctlgrs1057519962
Max Magnitude0
ClinVar
Risk rs1057519962(A;A) rs1057519962(T;T)
Alt rs1057519962(A;A) rs1057519962(T;T)
Reference Rs1057519962(G;G)
Significance Probable-Pathogenic
Disease Oesophageal carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Colorectal Neoplasms Adenocarcinoma of stomach Adenocarcinoma of prostate
Variation info
Gene SMAD4
CLNDBN Oesophageal carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Colorectal Neoplasms Adenocarcinoma of stomach Adenocarcinoma of prostate
Reversed 0
HGVS NC_000018.9:g.48593405G>A; NC_000018.9:g.48593405G>T
CLNSRC
CLNACC RCV000419978.1, RCV000421895.1, RCV000429536.1, RCV000430240.1, RCV000439617.1, RCV000439753.1, RCV000421325.1, RCV000421536.1, RCV000431585.1, RCV000434360.1, RCV000439155.1, RCV000444559.1,