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rs786205681

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205681(A;C)
Make rs786205681(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position75576799
GenePOLK
is asnp
is mentioned by
dbSNPrs786205681
ebirs786205681
HLIrs786205681
Exacrs786205681
Varsomers786205681
Maprs786205681
PheGenIrs786205681
hapmaprs786205681
1000 genomesrs786205681
hgdprs786205681
ensemblrs786205681
gopubmedrs786205681
geneviewrs786205681
scholarrs786205681
googlers786205681
pharmgkbrs786205681
gwascentralrs786205681
openSNPrs786205681
23andMers786205681
23andMe allrs786205681
SNP Nexus

SNPshotrs786205681
SNPdbers786205681
MSV3drs786205681
GWAS Ctlgrs786205681
Max Magnitude0
ClinVar
Risk rs786205681(C;C)
Alt rs786205681(C;C)
Reference rs786205681(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.75576799A>C
CLNSRC
CLNACC RCV000170545.1,