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rs4904947

From SNPedia

Orientationplus
Stabilizedplus
Make rs4904947(C;C)
Make rs4904947(C;T)
Make rs4904947(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position92505818
is asnp
is mentioned by
dbSNPrs4904947
ebirs4904947
HLIrs4904947
Exacrs4904947
Varsomers4904947
Maprs4904947
PheGenIrs4904947
hapmaprs4904947
1000 genomesrs4904947
hgdprs4904947
ensemblrs4904947
gopubmedrs4904947
geneviewrs4904947
scholarrs4904947
googlers4904947
pharmgkbrs4904947
gwascentralrs4904947
openSNPrs4904947
23andMers4904947
23andMe allrs4904947
SNP Nexus

SNPshotrs4904947
SNPdbers4904947
MSV3drs4904947
GWAS Ctlgrs4904947
GMAF0.2062
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21546767OA-icon.png]
Trait
Title Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes.
Risk Allele
P-val 0.000008
Odds Ratio 1.9000 [1.43-2.52]