rs6501384

Orientation

plus

Stabilized

plus

Make rs6501384(C;C)

Make rs6501384(C;T)

Make rs6501384(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

70294992

is a	snp
is	mentioned by
dbSNP	rs6501384
dbSNP (classic)	rs6501384
ClinGen	rs6501384
ebi	rs6501384
HLI	rs6501384
Exac	rs6501384
Gnomad	rs6501384
Varsome	rs6501384
LitVar	rs6501384
Map	rs6501384
PheGenI	rs6501384
Biobank	rs6501384
1000 genomes	rs6501384
hgdp	rs6501384
ensembl	rs6501384
geneview	rs6501384
scholar	rs6501384
google	rs6501384
pharmgkb	rs6501384
gwascentral	rs6501384
openSNP	rs6501384
23andMe	rs6501384
SNPshot	rs6501384
SNPdbe	rs6501384
MSV3d	rs6501384
GWAS Ctlg	rs6501384

GMAF

0.2934

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 20208534]
Trait	Eosinophilic esophagitis (pediatric)
Title	Common variants at 5q22 associate with pediatric eosinophilic esophagitis
Risk Allele	T
P-val	0.000006
Odds Ratio	1.41 [1.13-1.76]