Have questions? Visit https://www.reddit.com/r/SNPedia

rs5744857

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs5744857(A;A)
Make rs5744857(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position132659414
GenePOLE
is asnp
is mentioned by
dbSNPrs5744857
dbSNP (old)rs5744857
ClinGenrs5744857
ebirs5744857
HLIrs5744857
Exacrs5744857
Gnomadrs5744857
Varsomers5744857
Maprs5744857
PheGenIrs5744857
Biobankrs5744857
1000 genomesrs5744857
hgdprs5744857
ensemblrs5744857
gopubmedrs5744857
geneviewrs5744857
scholarrs5744857
googlers5744857
pharmgkbrs5744857
gwascentralrs5744857
openSNPrs5744857
23andMers5744857
23andMe allrs5744857
SNP Nexus

SNPshotrs5744857
SNPdbers5744857
MSV3drs5744857
GWAS Ctlgrs5744857
GMAF0.416
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20503108] VARS2 V552V variant as prognostic marker in patients with early breast cancer


ClinVar
Risk rs5744857(A;A)
Alt rs5744857(A;A)
Reference Rs5744857(G;G)
Significance Non-pathogenic
Disease not specified Hereditary cancer-predisposing syndrome
Variation info
Gene POLE
CLNDBN not specified Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000012.11:g.133236000C>T
CLNSRC
CLNACC RCV000421896.1, RCV000492265.1,