rs1033180

Orientation

plus

Stabilized

plus

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

Make rs1033180(C;T)

Make rs1033180(T;T)

Reference

GRCh37 37.1/131

Chromosome

6

Position

383546

is a	snp
is	mentioned by
dbSNP	rs1033180
dbSNP (classic)	rs1033180
ClinGen	rs1033180
ebi	rs1033180
HLI	rs1033180
Exac	rs1033180
Gnomad	rs1033180
Varsome	rs1033180
LitVar	rs1033180
Map	rs1033180
PheGenI	rs1033180
Biobank	rs1033180
1000 genomes	rs1033180
hgdp	rs1033180
ensembl	rs1033180
geneview	rs1033180
scholar	rs1033180
google	rs1033180
pharmgkb	rs1033180
gwascentral	rs1033180
openSNP	rs1033180
23andMe	rs1033180
SNPshot	rs1033180
SNPdbe	rs1033180
MSV3d	rs1033180
GWAS Ctlg	rs1033180

GMAF

0.03214

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	6E-8
Odds Ratio	1.21 [1.13-1.29]