rs4648011
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4648011(G;G) |
Make rs4648011(G;T) |
Make rs4648011(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 102554287 |
Gene | NFKB1 |
is a | snp |
is | mentioned by |
dbSNP | rs4648011 |
dbSNP (classic) | rs4648011 |
ClinGen | rs4648011 |
ebi | rs4648011 |
HLI | rs4648011 |
Exac | rs4648011 |
Gnomad | rs4648011 |
Varsome | rs4648011 |
LitVar | rs4648011 |
Map | rs4648011 |
PheGenI | rs4648011 |
Biobank | rs4648011 |
1000 genomes | rs4648011 |
hgdp | rs4648011 |
ensembl | rs4648011 |
geneview | rs4648011 |
scholar | rs4648011 |
rs4648011 | |
pharmgkb | rs4648011 |
gwascentral | rs4648011 |
openSNP | rs4648011 |
23andMe | rs4648011 |
SNPshot | rs4648011 |
SNPdbe | rs4648011 |
MSV3d | rs4648011 |
GWAS Ctlg | rs4648011 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 25397881] Intronic Variants in the NFKB1 Gene May Influence Hearing Forecast in Patients with Unilateral Sensorineural Hearing Loss in Meniere's Disease