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rs5910578

From SNPedia

Orientationplus
Stabilizedplus
Make rs5910578(C;C)
Make rs5910578(C;T)
Make rs5910578(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position119433739
GeneSLC25A43
is asnp
is mentioned by
dbSNPrs5910578
ebirs5910578
HLIrs5910578
Exacrs5910578
Varsomers5910578
Maprs5910578
PheGenIrs5910578
hapmaprs5910578
1000 genomesrs5910578
hgdprs5910578
ensemblrs5910578
gopubmedrs5910578
geneviewrs5910578
scholarrs5910578
googlers5910578
pharmgkbrs5910578
gwascentralrs5910578
openSNPrs5910578
23andMers5910578
23andMe allrs5910578
SNP Nexus

SNPshotrs5910578
SNPdbers5910578
MSV3drs5910578
GWAS Ctlgrs5910578
GMAF0.266
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21623375]
Trait
Title Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
Risk Allele C
P-val 1E-7
Odds Ratio 1.3400 [NR]