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rs11086243

From SNPedia

Orientationplus
Stabilizedplus
Make rs11086243(C;C)
Make rs11086243(C;T)
Make rs11086243(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position48150492
is asnp
is mentioned by
dbSNPrs11086243
ebirs11086243
HLIrs11086243
Exacrs11086243
Varsomers11086243
Maprs11086243
PheGenIrs11086243
hapmaprs11086243
1000 genomesrs11086243
hgdprs11086243
ensemblrs11086243
gopubmedrs11086243
geneviewrs11086243
scholarrs11086243
googlers11086243
pharmgkbrs11086243
gwascentralrs11086243
openSNPrs11086243
23andMers11086243
23andMe allrs11086243
SNP Nexus

SNPshotrs11086243
SNPdbers11086243
MSV3drs11086243
GWAS Ctlgrs11086243
GMAF0.3733
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21441931]
Trait
Title Common variation in GPC5 is associated with acquired nephrotic syndrome
Risk Allele T
P-val 0.000003
Odds Ratio 1.3700 [1.20-1.57]