rs17038828

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs17038828(C;T)

Make rs17038828(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

39433851

is a	snp
is	mentioned by
dbSNP	rs17038828
dbSNP (classic)	rs17038828
ClinGen	rs17038828
ebi	rs17038828
HLI	rs17038828
Exac	rs17038828
Gnomad	rs17038828
Varsome	rs17038828
LitVar	rs17038828
Map	rs17038828
PheGenI	rs17038828
Biobank	rs17038828
1000 genomes	rs17038828
hgdp	rs17038828
ensembl	rs17038828
geneview	rs17038828
scholar	rs17038828
google	rs17038828
pharmgkb	rs17038828
gwascentral	rs17038828
openSNP	rs17038828
23andMe	rs17038828
SNPshot	rs17038828
SNPdbe	rs17038828
MSV3d	rs17038828
GWAS Ctlg	rs17038828

GMAF

0.07071

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23382691]
Trait	IgG glycosylation
Title	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
Risk Allele	C
P-val	8E-6
Odds Ratio	.56 [0.31-0.81] unit decrease