rs4779031
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4779031(A;A) |
Make rs4779031(A;C) |
Make rs4779031(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 79241030 |
Gene | ANKRD34C-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs4779031 |
dbSNP (classic) | rs4779031 |
ClinGen | rs4779031 |
ebi | rs4779031 |
HLI | rs4779031 |
Exac | rs4779031 |
Gnomad | rs4779031 |
Varsome | rs4779031 |
LitVar | rs4779031 |
Map | rs4779031 |
PheGenI | rs4779031 |
Biobank | rs4779031 |
1000 genomes | rs4779031 |
hgdp | rs4779031 |
ensembl | rs4779031 |
geneview | rs4779031 |
scholar | rs4779031 |
rs4779031 | |
pharmgkb | rs4779031 |
gwascentral | rs4779031 |
openSNP | rs4779031 |
23andMe | rs4779031 |
SNPshot | rs4779031 |
SNPdbe | rs4779031 |
MSV3d | rs4779031 |
GWAS Ctlg | rs4779031 |
GMAF | 0.3324 |
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 | 2E-6 |
Odds Ratio | .18 [0.11-0.26] unit increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 15
- 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 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d