rs2664299
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2664299(A;A) |
Make rs2664299(A;G) |
Make rs2664299(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 99275850 |
is a | snp |
is | mentioned by |
dbSNP | rs2664299 |
dbSNP (classic) | rs2664299 |
ClinGen | rs2664299 |
ebi | rs2664299 |
HLI | rs2664299 |
Exac | rs2664299 |
Gnomad | rs2664299 |
Varsome | rs2664299 |
LitVar | rs2664299 |
Map | rs2664299 |
PheGenI | rs2664299 |
Biobank | rs2664299 |
1000 genomes | rs2664299 |
hgdp | rs2664299 |
ensembl | rs2664299 |
geneview | rs2664299 |
scholar | rs2664299 |
rs2664299 | |
pharmgkb | rs2664299 |
gwascentral | rs2664299 |
openSNP | rs2664299 |
23andMe | rs2664299 |
SNPshot | rs2664299 |
SNPdbe | rs2664299 |
MSV3d | rs2664299 |
GWAS Ctlg | rs2664299 |
GMAF | 0.2185 |
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 | C |
P-val | 9E-6 |
Odds Ratio | .17 [0.094-0.241] unit increase |