rs1957106
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1957106(A;A) |
Make rs1957106(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 35404564 |
Gene | NFKBIA |
is a | snp |
is | mentioned by |
dbSNP | rs1957106 |
dbSNP (classic) | rs1957106 |
ClinGen | rs1957106 |
ebi | rs1957106 |
HLI | rs1957106 |
Exac | rs1957106 |
Gnomad | rs1957106 |
Varsome | rs1957106 |
LitVar | rs1957106 |
Map | rs1957106 |
PheGenI | rs1957106 |
Biobank | rs1957106 |
1000 genomes | rs1957106 |
hgdp | rs1957106 |
ensembl | rs1957106 |
geneview | rs1957106 |
scholar | rs1957106 |
rs1957106 | |
pharmgkb | rs1957106 |
gwascentral | rs1957106 |
openSNP | rs1957106 |
23andMe | rs1957106 |
SNPshot | rs1957106 |
SNPdbe | rs1957106 |
MSV3d | rs1957106 |
GWAS Ctlg | rs1957106 |
GMAF | 0.2406 |
Max Magnitude | 0 |
[PMID 19500386] Polymorphisms in NF-kappaB Inhibitors and Risk of Epithelial Ovarian Cancer
[PMID 19223558] Polymorphic variation in NFKB1 and other aspirin-related genes and risk of Hodgkin lymphoma.
[PMID 25215581] Identification of a NFKBIA polymorphism associated with lower NFKBIA protein levels and poor survival outcomes in patients with glioblastoma multiforme
ClinVar | |
---|---|
Risk | rs1957106(A;A) |
Alt | rs1957106(A;A) |
Reference | Rs1957106(G;G) |
Significance | Non-pathogenic |
Disease | Ectodermal dysplasia not specified |
Variation | info |
Gene | NFKBIA |
CLNDBN | Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant not specified |
Reversed | 0 |
HGVS | NC_000014.8:g.35873770G>A |
CLNSRC | |
CLNACC | RCV000284527.1, RCV000455089.1, |