rs4899260

Orientation

plus

Stabilized

plus

Make rs4899260(C;C)

Make rs4899260(C;T)

Make rs4899260(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

68811487

is a	snp
is	mentioned by
dbSNP	rs4899260
dbSNP (classic)	rs4899260
ClinGen	rs4899260
ebi	rs4899260
HLI	rs4899260
Exac	rs4899260
Gnomad	rs4899260
Varsome	rs4899260
LitVar	rs4899260
Map	rs4899260
PheGenI	rs4899260
Biobank	rs4899260
1000 genomes	rs4899260
hgdp	rs4899260
ensembl	rs4899260
geneview	rs4899260
scholar	rs4899260
google	rs4899260
pharmgkb	rs4899260
gwascentral	rs4899260
openSNP	rs4899260
23andMe	rs4899260
SNPshot	rs4899260
SNPdbe	rs4899260
MSV3d	rs4899260
GWAS Ctlg	rs4899260

GMAF

0.1988

Max Magnitude

0

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

GWAS snp
PMID	[PMID 20190752]
Trait	Celiac disease
Title	Multiple common variants for celiac disease influencing immune gene expression
Risk Allele	A
P-val	4E-7
Odds Ratio	1.12 [1.07-1.16]