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rs7179432

From SNPedia

Orientationplus
Stabilizedplus
Make rs7179432(C;C)
Make rs7179432(C;T)
Make rs7179432(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position93021742
GeneCHD2
is asnp
is mentioned by
dbSNPrs7179432
dbSNP (classic)rs7179432
ClinGenrs7179432
ebirs7179432
HLIrs7179432
Exacrs7179432
Gnomadrs7179432
Varsomers7179432
LitVarrs7179432
Maprs7179432
PheGenIrs7179432
Biobankrs7179432
1000 genomesrs7179432
hgdprs7179432
ensemblrs7179432
geneviewrs7179432
scholarrs7179432
googlers7179432
pharmgkbrs7179432
gwascentralrs7179432
openSNPrs7179432
23andMers7179432
SNPshotrs7179432
SNPdbers7179432
MSV3drs7179432
GWAS Ctlgrs7179432
GMAF0.4376
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23382691OA-icon.png]
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 4E-6
Odds Ratio .16 [0.09-0.224] unit decrease