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rs1057519739

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519739(A;A)
Make rs1057519739(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position51065518
GeneSMAD4
is asnp
is mentioned by
dbSNPrs1057519739
dbSNP (old)rs1057519739
ClinGenrs1057519739
ebirs1057519739
HLIrs1057519739
Exacrs1057519739
Gnomadrs1057519739
Varsomers1057519739
LitVarrs1057519739
Maprs1057519739
PheGenIrs1057519739
Biobankrs1057519739
1000 genomesrs1057519739
hgdprs1057519739
ensemblrs1057519739
gopubmedrs1057519739
geneviewrs1057519739
scholarrs1057519739
googlers1057519739
pharmgkbrs1057519739
gwascentralrs1057519739
openSNPrs1057519739
23andMers1057519739
23andMe allrs1057519739
SNPshotrs1057519739
SNPdbers1057519739
MSV3drs1057519739
GWAS Ctlgrs1057519739
Max Magnitude0
ClinVar
Risk rs1057519739(A;A) rs1057519739(C;C)
Alt rs1057519739(A;A) rs1057519739(C;C)
Reference Rs1057519739(G;G)
Significance Pathogenic
Disease Colorectal Neoplasms
Variation info
Gene SMAD4
CLNDBN Colorectal Neoplasms
Reversed 0
HGVS NC_000018.9:g.48591888G>A; NC_000018.9:g.48591888G>C
CLNSRC
CLNACC RCV000444906.1, RCV000427066.1,