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rs10498635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs10498635(C;T)
Make rs10498635(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position92636964
GeneRIN3
is asnp
is mentioned by
dbSNPrs10498635
ebirs10498635
HLIrs10498635
Exacrs10498635
Varsomers10498635
Maprs10498635
PheGenIrs10498635
hapmaprs10498635
1000 genomesrs10498635
hgdprs10498635
ensemblrs10498635
gopubmedrs10498635
geneviewrs10498635
scholarrs10498635
googlers10498635
pharmgkbrs10498635
gwascentralrs10498635
openSNPrs10498635
23andMers10498635
23andMe allrs10498635
SNP Nexus

SNPshotrs10498635
SNPdbers10498635
MSV3drs10498635
GWAS Ctlgrs10498635
GMAF0.09826
Max Magnitude0
? (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 3E-11
Odds Ratio 1.4400 [1.29-1.60]