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rs786205692

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205692(A;G)
Make rs786205692(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position75593998
GenePOLK
is asnp
is mentioned by
dbSNPrs786205692
ebirs786205692
HLIrs786205692
Exacrs786205692
Varsomers786205692
Maprs786205692
PheGenIrs786205692
hapmaprs786205692
1000 genomesrs786205692
hgdprs786205692
ensemblrs786205692
gopubmedrs786205692
geneviewrs786205692
scholarrs786205692
googlers786205692
pharmgkbrs786205692
gwascentralrs786205692
openSNPrs786205692
23andMers786205692
23andMe allrs786205692
SNP Nexus

SNPshotrs786205692
SNPdbers786205692
MSV3drs786205692
GWAS Ctlgrs786205692
Max Magnitude0
ClinVar
Risk rs786205692(G;G)
Alt rs786205692(G;G)
Reference rs786205692(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.75593998A>G
CLNSRC
CLNACC RCV000170561.1,