Have questions? Visit https://www.reddit.com/r/SNPedia

rs16844841

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs16844841(A;C)
Make rs16844841(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position225402973
GeneLBR
is asnp
is mentioned by
dbSNPrs16844841
dbSNP (classic)rs16844841
ClinGenrs16844841
ebirs16844841
HLIrs16844841
Exacrs16844841
Gnomadrs16844841
Varsomers16844841
LitVarrs16844841
Maprs16844841
PheGenIrs16844841
Biobankrs16844841
1000 genomesrs16844841
hgdprs16844841
ensemblrs16844841
geneviewrs16844841
scholarrs16844841
googlers16844841
pharmgkbrs16844841
gwascentralrs16844841
openSNPrs16844841
23andMers16844841
SNPshotrs16844841
SNPdbers16844841
MSV3drs16844841
GWAS Ctlgrs16844841
GMAF0.03627
Max Magnitude0
? (A;A) (A;C) (C;C) 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 .32 [0.18-0.45] unit increase


ClinVar
Risk rs16844841(C;C)
Alt rs16844841(C;C)
Reference Rs16844841(A;A)
Significance Probable-non-pathogenic
Disease Greenberg dysplasia
Variation info
Gene LBR
CLNDBN Greenberg dysplasia
Reversed 0
HGVS NC_000001.10:g.225590675A>C
CLNSRC
CLNACC RCV000290340.1,