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rs980578884

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs980578884(A;A)
Make rs980578884(A;G)
Make rs980578884(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position132673217
GenePOLE
is asnp
is mentioned by
dbSNPrs980578884
dbSNP (classic)rs980578884
ClinGenrs980578884
ebirs980578884
HLIrs980578884
Exacrs980578884
Gnomadrs980578884
Varsomers980578884
LitVarrs980578884
Maprs980578884
PheGenIrs980578884
Biobankrs980578884
1000 genomesrs980578884
hgdprs980578884
ensemblrs980578884
geneviewrs980578884
scholarrs980578884
googlers980578884
pharmgkbrs980578884
gwascentralrs980578884
openSNPrs980578884
23andMers980578884
SNPshotrs980578884
SNPdbers980578884
MSV3drs980578884
GWAS Ctlgrs980578884
Max Magnitude0
ClinVar
Risk rs980578884(T;T)
Alt rs980578884(T;T)
Reference Rs980578884(C;C)
Significance Pathogenic
Disease Colorectal cancer
Variation info
Gene POLE
CLNDBN Colorectal cancer, susceptibility to, 12
Reversed 0
HGVS NC_000012.11:g.133249803C>T
CLNSRC
CLNACC RCV000417197.1,