rs12367448

Orientation

plus

Stabilized

plus

Make rs12367448(A;A)

Make rs12367448(A;C)

Make rs12367448(C;C)

Reference

GRCh38 38.1/141

Chromosome

12

Position

69187442

is a	snp
is	mentioned by
dbSNP	rs12367448
dbSNP (classic)	rs12367448
ClinGen	rs12367448
ebi	rs12367448
HLI	rs12367448
Exac	rs12367448
Gnomad	rs12367448
Varsome	rs12367448
LitVar	rs12367448
Map	rs12367448
PheGenI	rs12367448
Biobank	rs12367448
1000 genomes	rs12367448
hgdp	rs12367448
ensembl	rs12367448
geneview	rs12367448
scholar	rs12367448
google	rs12367448
pharmgkb	rs12367448
gwascentral	rs12367448
openSNP	rs12367448
23andMe	rs12367448
SNPshot	rs12367448
SNPdbe	rs12367448
MSV3d	rs12367448
GWAS Ctlg	rs12367448

GMAF

0.1263

Max Magnitude

0

?	(A;A) (A;C) (C;C)	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	6E-6
Odds Ratio	.25 [0.14-0.35] unit increase