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rs9310709

From SNPedia

Orientationplus
Stabilizedplus
Make rs9310709(C;C)
Make rs9310709(C;T)
Make rs9310709(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position23052083
is asnp
is mentioned by
dbSNPrs9310709
dbSNP (classic)rs9310709
ClinGenrs9310709
ebirs9310709
HLIrs9310709
Exacrs9310709
Gnomadrs9310709
Varsomers9310709
LitVarrs9310709
Maprs9310709
PheGenIrs9310709
Biobankrs9310709
1000 genomesrs9310709
hgdprs9310709
ensemblrs9310709
geneviewrs9310709
scholarrs9310709
googlers9310709
pharmgkbrs9310709
gwascentralrs9310709
openSNPrs9310709
23andMers9310709
SNPshotrs9310709
SNPdbers9310709
MSV3drs9310709
GWAS Ctlgrs9310709
GMAF0.416
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 20686651OA-icon.png]
Trait
Title Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases
Risk Allele C
P-val 0.000002
Odds Ratio 1.15 [1.09-1.22]

This SNP is reportedly associated with chronic kidney disease and kidney stones. [PMID 20686651OA-icon.png]