rs4958881
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common/normal |
Make rs4958881(C;C) |
Make rs4958881(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 151070675 |
Gene | TNIP1 |
is a | snp |
is | mentioned by |
dbSNP | rs4958881 |
dbSNP (classic) | rs4958881 |
ClinGen | rs4958881 |
ebi | rs4958881 |
HLI | rs4958881 |
Exac | rs4958881 |
Gnomad | rs4958881 |
Varsome | rs4958881 |
LitVar | rs4958881 |
Map | rs4958881 |
PheGenI | rs4958881 |
Biobank | rs4958881 |
1000 genomes | rs4958881 |
hgdp | rs4958881 |
ensembl | rs4958881 |
geneview | rs4958881 |
scholar | rs4958881 |
rs4958881 | |
pharmgkb | rs4958881 |
gwascentral | rs4958881 |
openSNP | rs4958881 |
23andMe | rs4958881 |
SNPshot | rs4958881 |
SNPdbe | rs4958881 |
MSV3d | rs4958881 |
GWAS Ctlg | rs4958881 |
GMAF | 0.1938 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22896740] Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study
GWAS snp | |
---|---|
PMID | [PMID 23055271![]() |
Trait | Myasthenia gravis |
Title | Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. |
Risk Allele | G |
P-val | 3E-10 |
Odds Ratio | 1.73 [1.46-2.06] |