rs7661864
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7661864(A;A) |
Make rs7661864(A;G) |
Make rs7661864(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 6734638 |
is a | snp |
is | mentioned by |
dbSNP | rs7661864 |
dbSNP (classic) | rs7661864 |
ClinGen | rs7661864 |
ebi | rs7661864 |
HLI | rs7661864 |
Exac | rs7661864 |
Gnomad | rs7661864 |
Varsome | rs7661864 |
LitVar | rs7661864 |
Map | rs7661864 |
PheGenI | rs7661864 |
Biobank | rs7661864 |
1000 genomes | rs7661864 |
hgdp | rs7661864 |
ensembl | rs7661864 |
geneview | rs7661864 |
scholar | rs7661864 |
rs7661864 | |
pharmgkb | rs7661864 |
gwascentral | rs7661864 |
openSNP | rs7661864 |
23andMe | rs7661864 |
SNPshot | rs7661864 |
SNPdbe | rs7661864 |
MSV3d | rs7661864 |
GWAS Ctlg | rs7661864 |
GMAF | 0.3361 |
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 | 5E-6 |
Odds Ratio | .33 [0.19-0.47] unit increase |