rs16844841
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs16844841(A;C) |
Make rs16844841(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 225402973 |
Gene | LBR |
is a | snp |
is | mentioned by |
dbSNP | rs16844841 |
dbSNP (classic) | rs16844841 |
ClinGen | rs16844841 |
ebi | rs16844841 |
HLI | rs16844841 |
Exac | rs16844841 |
Gnomad | rs16844841 |
Varsome | rs16844841 |
LitVar | rs16844841 |
Map | rs16844841 |
PheGenI | rs16844841 |
Biobank | rs16844841 |
1000 genomes | rs16844841 |
hgdp | rs16844841 |
ensembl | rs16844841 |
geneview | rs16844841 |
scholar | rs16844841 |
rs16844841 | |
pharmgkb | rs16844841 |
gwascentral | rs16844841 |
openSNP | rs16844841 |
23andMe | rs16844841 |
SNPshot | rs16844841 |
SNPdbe | rs16844841 |
MSV3d | rs16844841 |
GWAS Ctlg | rs16844841 |
GMAF | 0.03627 |
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 | 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, |