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rs786205694

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205694(G;G)
Make rs786205694(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position75598099
GenePOLK
is asnp
is mentioned by
dbSNPrs786205694
ebirs786205694
HLIrs786205694
Exacrs786205694
Varsomers786205694
Maprs786205694
PheGenIrs786205694
hapmaprs786205694
1000 genomesrs786205694
hgdprs786205694
ensemblrs786205694
gopubmedrs786205694
geneviewrs786205694
scholarrs786205694
googlers786205694
pharmgkbrs786205694
gwascentralrs786205694
openSNPrs786205694
23andMers786205694
23andMe allrs786205694
SNP Nexus

SNPshotrs786205694
SNPdbers786205694
MSV3drs786205694
GWAS Ctlgrs786205694
Max Magnitude0
ClinVar
Risk rs786205694(G;G)
Alt rs786205694(G;G)
Reference rs786205694(T;T)
Significance Pathogenic
Disease Malignant tumor of prostate
Variation info
Gene POLK
CLNDBN Malignant tumor of prostate
Reversed 0
HGVS NC_000005.10:g.75598099T>G
CLNSRC
CLNACC RCV000170563.1,