rs6721181

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs6721181(C;T)

Make rs6721181(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

39888556

is a	snp
is	mentioned by
dbSNP	rs6721181
dbSNP (classic)	rs6721181
ClinGen	rs6721181
ebi	rs6721181
HLI	rs6721181
Exac	rs6721181
Gnomad	rs6721181
Varsome	rs6721181
LitVar	rs6721181
Map	rs6721181
PheGenI	rs6721181
Biobank	rs6721181
1000 genomes	rs6721181
hgdp	rs6721181
ensembl	rs6721181
geneview	rs6721181
scholar	rs6721181
google	rs6721181
pharmgkb	rs6721181
gwascentral	rs6721181
openSNP	rs6721181
23andMe	rs6721181
SNPshot	rs6721181
SNPdbe	rs6721181
MSV3d	rs6721181
GWAS Ctlg	rs6721181

GMAF

0.01607

Max Magnitude

0

?	(C;C) (C;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	6E-7
Odds Ratio	NR NR