rs11989782

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;C)	0	common in complete genomics

Make rs11989782(A;A)

Make rs11989782(C;C)

Reference

GRCh38 38.1/141

Chromosome

8

Position

120682410

Gene

SNTB1

is a	snp
is	mentioned by
dbSNP	rs11989782
dbSNP (classic)	rs11989782
ClinGen	rs11989782
ebi	rs11989782
HLI	rs11989782
Exac	rs11989782
Gnomad	rs11989782
Varsome	rs11989782
LitVar	rs11989782
Map	rs11989782
PheGenI	rs11989782
Biobank	rs11989782
1000 genomes	rs11989782
hgdp	rs11989782
ensembl	rs11989782
geneview	rs11989782
scholar	rs11989782
google	rs11989782
pharmgkb	rs11989782
gwascentral	rs11989782
openSNP	rs11989782
23andMe	rs11989782
SNPshot	rs11989782
SNPdbe	rs11989782
MSV3d	rs11989782
GWAS Ctlg	rs11989782

GMAF

0.14

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

GWAS snp
PMID	[PMID 20208534]
Trait	Eosinophilic esophagitis (pediatric)
Title	Common variants at 5q22 associate with pediatric eosinophilic esophagitis
Risk Allele	A
P-val	0.000007
Odds Ratio	1.53 [1.21-1.93]