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rs10498792

From SNPedia

Orientationplus
Stabilizedplus
Make rs10498792(C;C)
Make rs10498792(C;T)
Make rs10498792(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position51801833
GenePKHD1
is asnp
is mentioned by
dbSNPrs10498792
ebirs10498792
HLIrs10498792
Exacrs10498792
Varsomers10498792
Maprs10498792
PheGenIrs10498792
hapmaprs10498792
1000 genomesrs10498792
hgdprs10498792
ensemblrs10498792
gopubmedrs10498792
geneviewrs10498792
scholarrs10498792
googlers10498792
pharmgkbrs10498792
gwascentralrs10498792
openSNPrs10498792
23andMers10498792
23andMe allrs10498792
SNP Nexus

SNPshotrs10498792
SNPdbers10498792
MSV3drs10498792
GWAS Ctlgrs10498792
GMAF0.1625
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs10498792
PubMedID [PMID 17903305OA-icon.png]
Condition Prostate cancer
Gene PKHD1
Risk Allele
pValue 3.00E-006
OR NA
95% CI



GET Evidence
rs10498792
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary