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rs786205691

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205691(A;T)
Make rs786205691(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position75596481
GenePOLK
is asnp
is mentioned by
dbSNPrs786205691
ebirs786205691
HLIrs786205691
Exacrs786205691
Varsomers786205691
Maprs786205691
PheGenIrs786205691
hapmaprs786205691
1000 genomesrs786205691
hgdprs786205691
ensemblrs786205691
gopubmedrs786205691
geneviewrs786205691
scholarrs786205691
googlers786205691
pharmgkbrs786205691
gwascentralrs786205691
openSNPrs786205691
23andMers786205691
23andMe allrs786205691
SNP Nexus

SNPshotrs786205691
SNPdbers786205691
MSV3drs786205691
GWAS Ctlgrs786205691
Max Magnitude0
ClinVar
Risk rs786205691(T;T)
Alt rs786205691(T;T)
Reference rs786205691(A;A)
Significance Pathogenic
Disease Malignant tumor of prostate
Variation info
Gene POLK
CLNDBN Malignant tumor of prostate
Reversed 0
HGVS NC_000005.10:g.75596481A>T
CLNSRC
CLNACC RCV000170559.1,