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rs13070584

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs13070584(C;T)
Make rs13070584(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position99547493
is asnp
is mentioned by
dbSNPrs13070584
ebirs13070584
HLIrs13070584
Exacrs13070584
Varsomers13070584
Maprs13070584
PheGenIrs13070584
hapmaprs13070584
1000 genomesrs13070584
hgdprs13070584
ensemblrs13070584
gopubmedrs13070584
geneviewrs13070584
scholarrs13070584
googlers13070584
pharmgkbrs13070584
gwascentralrs13070584
openSNPrs13070584
23andMers13070584
23andMe allrs13070584
SNP Nexus

SNPshotrs13070584
SNPdbers13070584
MSV3drs13070584
GWAS Ctlgrs13070584
GMAF0.07759
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 T
P-val 0.000002
Odds Ratio 1.42 [1.23-1.65]

The T allele of rs13070584 has been associated with chronic kidney disease and kidney stones. [PMID 20686651OA-icon.png]