rs626657
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs626657(A;A) |
Make rs626657(A;C) |
Make rs626657(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 39176710 |
Gene | CACNB1, LOC105371768 |
is a | snp |
is | mentioned by |
dbSNP | rs626657 |
dbSNP (classic) | rs626657 |
ClinGen | rs626657 |
ebi | rs626657 |
HLI | rs626657 |
Exac | rs626657 |
Gnomad | rs626657 |
Varsome | rs626657 |
LitVar | rs626657 |
Map | rs626657 |
PheGenI | rs626657 |
Biobank | rs626657 |
1000 genomes | rs626657 |
hgdp | rs626657 |
ensembl | rs626657 |
geneview | rs626657 |
scholar | rs626657 |
rs626657 | |
pharmgkb | rs626657 |
gwascentral | rs626657 |
openSNP | rs626657 |
23andMe | rs626657 |
SNPshot | rs626657 |
SNPdbe | rs626657 |
MSV3d | rs626657 |
GWAS Ctlg | rs626657 |
GMAF | 0.2571 |
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 | .23 [0.14-0.33] unit decrease |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 17
- 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 HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d