rs17033506

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs17033506(G;T)

Make rs17033506(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

35598334

is a	snp
is	mentioned by
dbSNP	rs17033506
dbSNP (classic)	rs17033506
ClinGen	rs17033506
ebi	rs17033506
HLI	rs17033506
Exac	rs17033506
Gnomad	rs17033506
Varsome	rs17033506
LitVar	rs17033506
Map	rs17033506
PheGenI	rs17033506
Biobank	rs17033506
1000 genomes	rs17033506
hgdp	rs17033506
ensembl	rs17033506
geneview	rs17033506
scholar	rs17033506
google	rs17033506
pharmgkb	rs17033506
gwascentral	rs17033506
openSNP	rs17033506
23andMe	rs17033506
SNPshot	rs17033506
SNPdbe	rs17033506
MSV3d	rs17033506
GWAS Ctlg	rs17033506

GMAF

0.03581

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

GWAS snp
PMID	[PMID 23829686]
Trait	Asthma (childhood onset)
Title	Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations.
Risk Allele
P-val	4E-7
Odds Ratio	NR NR