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rs1057519945

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519945(G;T)
Make rs1057519945(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position132673703
GenePOLE
is asnp
is mentioned by
dbSNPrs1057519945
dbSNP (old)rs1057519945
ClinGenrs1057519945
ebirs1057519945
HLIrs1057519945
Exacrs1057519945
Gnomadrs1057519945
Varsomers1057519945
Maprs1057519945
PheGenIrs1057519945
Biobankrs1057519945
1000 genomesrs1057519945
hgdprs1057519945
ensemblrs1057519945
gopubmedrs1057519945
geneviewrs1057519945
scholarrs1057519945
googlers1057519945
pharmgkbrs1057519945
gwascentralrs1057519945
openSNPrs1057519945
23andMers1057519945
23andMe allrs1057519945
SNPshotrs1057519945
SNPdbers1057519945
MSV3drs1057519945
GWAS Ctlgrs1057519945
Max Magnitude0
ClinVar
Risk rs1057519945(T;T)
Alt rs1057519945(T;T)
Reference Rs1057519945(G;G)
Significance Probable-Pathogenic
Disease Malignant neoplasm of body of uterus Adenocarcinoma of stomach Colorectal Neoplasms Glioblastoma
Variation info
Gene POLE
CLNDBN Malignant neoplasm of body of uterus Adenocarcinoma of stomach Colorectal Neoplasms Glioblastoma
Reversed 1
HGVS NC_000012.11:g.133250289C>A
CLNSRC
CLNACC RCV000423521.1, RCV000424174.1, RCV000434429.1, RCV000441211.1,