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rs1058065

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1058065(C;T)
Make rs1058065(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position27364857
GeneEIF2B4
is asnp
is mentioned by
dbSNPrs1058065
ebirs1058065
HLIrs1058065
Exacrs1058065
Varsomers1058065
Maprs1058065
PheGenIrs1058065
hapmaprs1058065
1000 genomesrs1058065
hgdprs1058065
ensemblrs1058065
gopubmedrs1058065
geneviewrs1058065
scholarrs1058065
googlers1058065
pharmgkbrs1058065
gwascentralrs1058065
openSNPrs1058065
23andMers1058065
23andMe allrs1058065
SNP Nexus

SNPshotrs1058065
SNPdbers1058065
MSV3drs1058065
GWAS Ctlgrs1058065
GMAF0.008264
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 G
P-val 4E-6
Odds Ratio .54 [0.31-0.77] unit increase


ClinVar
Risk rs1058065(T;T)
Alt rs1058065(T;T)
Reference rs1058065(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene EIF2B4
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.27587724G>A
CLNSRC ClinVar Emory University
CLNACC RCV000081779.4,