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rs2200578

From SNPedia

Orientationplus
Stabilizedplus
Make rs2200578(C;C)
Make rs2200578(C;T)
Make rs2200578(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position99259781
is asnp
is mentioned by
dbSNPrs2200578
dbSNP (classic)rs2200578
ClinGenrs2200578
ebirs2200578
HLIrs2200578
Exacrs2200578
Gnomadrs2200578
Varsomers2200578
LitVarrs2200578
Maprs2200578
PheGenIrs2200578
Biobankrs2200578
1000 genomesrs2200578
hgdprs2200578
ensemblrs2200578
geneviewrs2200578
scholarrs2200578
googlers2200578
pharmgkbrs2200578
gwascentralrs2200578
openSNPrs2200578
23andMers2200578
SNPshotrs2200578
SNPdbers2200578
MSV3drs2200578
GWAS Ctlgrs2200578
GMAF0.208
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-7
Odds Ratio .19 [0.12-0.26] unit decrease