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rs10494112

From SNPedia

Orientationplus
Stabilizedplus
Make rs10494112(A;A)
Make rs10494112(A;G)
Make rs10494112(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position109809855
is asnp
is mentioned by
dbSNPrs10494112
ebirs10494112
HLIrs10494112
Exacrs10494112
Varsomers10494112
Maprs10494112
PheGenIrs10494112
hapmaprs10494112
1000 genomesrs10494112
hgdprs10494112
ensemblrs10494112
gopubmedrs10494112
geneviewrs10494112
scholarrs10494112
googlers10494112
pharmgkbrs10494112
gwascentralrs10494112
openSNPrs10494112
23andMers10494112
23andMe allrs10494112
SNP Nexus

SNPshotrs10494112
SNPdbers10494112
MSV3drs10494112
GWAS Ctlgrs10494112
GMAF0.1244
Max Magnitude
? (A;A) (A;G) (G;G) 28
related to Paget’s disease of bone 23andMe blog.
GWAS snp
PMID [PMID 21623375]
Trait
Title Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
Risk Allele G
P-val 7E-35
Odds Ratio 1.7200 [1.57-1.87]