rs11619878
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11619878(A;A) |
Make rs11619878(A;G) |
Make rs11619878(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 65637888 |
is a | snp |
is | mentioned by |
dbSNP | rs11619878 |
dbSNP (classic) | rs11619878 |
ClinGen | rs11619878 |
ebi | rs11619878 |
HLI | rs11619878 |
Exac | rs11619878 |
Gnomad | rs11619878 |
Varsome | rs11619878 |
LitVar | rs11619878 |
Map | rs11619878 |
PheGenI | rs11619878 |
Biobank | rs11619878 |
1000 genomes | rs11619878 |
hgdp | rs11619878 |
ensembl | rs11619878 |
geneview | rs11619878 |
scholar | rs11619878 |
rs11619878 | |
pharmgkb | rs11619878 |
gwascentral | rs11619878 |
openSNP | rs11619878 |
23andMe | rs11619878 |
SNPshot | rs11619878 |
SNPdbe | rs11619878 |
MSV3d | rs11619878 |
GWAS Ctlg | rs11619878 |
GMAF | 0.3719 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | G |
P-val | 1E-7 |
Odds Ratio | .16 [0.1-0.22] unit decrease |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 13
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d