rs1958589

Orientation

plus

Stabilized

plus

Make rs1958589(C;C)

Make rs1958589(C;T)

Make rs1958589(T;T)

Reference

GRCh38 38.1/142

Chromosome

14

Position

34375170

is a	snp
is	mentioned by
dbSNP	rs1958589
dbSNP (classic)	rs1958589
ClinGen	rs1958589
ebi	rs1958589
HLI	rs1958589
Exac	rs1958589
Gnomad	rs1958589
Varsome	rs1958589
LitVar	rs1958589
Map	rs1958589
PheGenI	rs1958589
Biobank	rs1958589
1000 genomes	rs1958589
hgdp	rs1958589
ensembl	rs1958589
geneview	rs1958589
scholar	rs1958589
google	rs1958589
pharmgkb	rs1958589
gwascentral	rs1958589
openSNP	rs1958589
23andMe	rs1958589
SNPshot	rs1958589
SNPdbe	rs1958589
MSV3d	rs1958589
GWAS Ctlg	rs1958589

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23936387]
Trait	Celiac disease
Title	A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
Risk Allele	C
P-val	4E-6
Odds Ratio	NR NR