rs11078697
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs11078697(C;T) |
Make rs11078697(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 7565912 |
Gene | SENP3, SENP3-EIF4A1 |
is a | snp |
is | mentioned by |
dbSNP | rs11078697 |
dbSNP (classic) | rs11078697 |
ClinGen | rs11078697 |
ebi | rs11078697 |
HLI | rs11078697 |
Exac | rs11078697 |
Gnomad | rs11078697 |
Varsome | rs11078697 |
LitVar | rs11078697 |
Map | rs11078697 |
PheGenI | rs11078697 |
Biobank | rs11078697 |
1000 genomes | rs11078697 |
hgdp | rs11078697 |
ensembl | rs11078697 |
geneview | rs11078697 |
scholar | rs11078697 |
rs11078697 | |
pharmgkb | rs11078697 |
gwascentral | rs11078697 |
openSNP | rs11078697 |
23andMe | rs11078697 |
SNPshot | rs11078697 |
SNPdbe | rs11078697 |
MSV3d | rs11078697 |
GWAS Ctlg | rs11078697 |
GMAF | 0.08724 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23118916![]() |
Trait | IgM levels |
Title | Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population. |
Risk Allele | C |
P-val | 4E-7 |
Odds Ratio | NR NR |