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rs1057519944

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519944(C;T)
Make rs1057519944(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position132676599
GenePOLE
is asnp
is mentioned by
dbSNPrs1057519944
dbSNP (old)rs1057519944
ClinGenrs1057519944
ebirs1057519944
HLIrs1057519944
Exacrs1057519944
Gnomadrs1057519944
Varsomers1057519944
Maprs1057519944
PheGenIrs1057519944
Biobankrs1057519944
1000 genomesrs1057519944
hgdprs1057519944
ensemblrs1057519944
gopubmedrs1057519944
geneviewrs1057519944
scholarrs1057519944
googlers1057519944
pharmgkbrs1057519944
gwascentralrs1057519944
openSNPrs1057519944
23andMers1057519944
23andMe allrs1057519944
SNPshotrs1057519944
SNPdbers1057519944
MSV3drs1057519944
GWAS Ctlgrs1057519944
Max Magnitude0
ClinVar
Risk rs1057519944(T;T)
Alt rs1057519944(T;T)
Reference Rs1057519944(C;C)
Significance Probable-Pathogenic
Disease Pancreatic adenocarcinoma Colorectal Neoplasms Neoplasm of breast Uterine Carcinosarcoma Malignant neoplasm of body of uterus
Variation info
Gene POLE
CLNDBN Pancreatic adenocarcinoma Colorectal Neoplasms Neoplasm of breast Uterine Carcinosarcoma Malignant neoplasm of body of uterus
Reversed 1
HGVS NC_000012.11:g.133253185G>A
CLNSRC
CLNACC RCV000418641.1, RCV000419260.1, RCV000429545.1, RCV000436302.1, RCV000436940.1,