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rs786205693

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205693(A;C)
Make rs786205693(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position75596249
GenePOLK
is asnp
is mentioned by
dbSNPrs786205693
ebirs786205693
HLIrs786205693
Exacrs786205693
Varsomers786205693
Maprs786205693
PheGenIrs786205693
hapmaprs786205693
1000 genomesrs786205693
hgdprs786205693
ensemblrs786205693
gopubmedrs786205693
geneviewrs786205693
scholarrs786205693
googlers786205693
pharmgkbrs786205693
gwascentralrs786205693
openSNPrs786205693
23andMers786205693
23andMe allrs786205693
SNP Nexus

SNPshotrs786205693
SNPdbers786205693
MSV3drs786205693
GWAS Ctlgrs786205693
Max Magnitude0
ClinVar
Risk rs786205693(C;C)
Alt rs786205693(C;C)
Reference rs786205693(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.75596249A>C
CLNSRC
CLNACC RCV000170562.1,