rs10498635

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common on affy axiom data

Make rs10498635(C;T)

Make rs10498635(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

92636964

Gene

RIN3

is a	snp
is	mentioned by
dbSNP	rs10498635
dbSNP (classic)	rs10498635
ClinGen	rs10498635
ebi	rs10498635
HLI	rs10498635
Exac	rs10498635
Gnomad	rs10498635
Varsome	rs10498635
LitVar	rs10498635
Map	rs10498635
PheGenI	rs10498635
Biobank	rs10498635
1000 genomes	rs10498635
hgdp	rs10498635
ensembl	rs10498635
geneview	rs10498635
scholar	rs10498635
google	rs10498635
pharmgkb	rs10498635
gwascentral	rs10498635
openSNP	rs10498635
23andMe	rs10498635
SNPshot	rs10498635
SNPdbe	rs10498635
MSV3d	rs10498635
GWAS Ctlg	rs10498635

GMAF

0.09826

Max Magnitude

0

?	(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]