rs1401880558
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;T) | 3 | Carrier of a DFNB7/11 deafness mutation |
Make rs1401880558(C;G) |
Make rs1401880558(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 72789264 |
Gene | TMC1 |
is a | snp |
is | mentioned by |
dbSNP | rs1401880558 |
dbSNP (classic) | rs1401880558 |
ClinGen | rs1401880558 |
ebi | rs1401880558 |
HLI | rs1401880558 |
Exac | rs1401880558 |
Gnomad | rs1401880558 |
Varsome | rs1401880558 |
LitVar | rs1401880558 |
Map | rs1401880558 |
PheGenI | rs1401880558 |
Biobank | rs1401880558 |
1000 genomes | rs1401880558 |
hgdp | rs1401880558 |
ensembl | rs1401880558 |
geneview | rs1401880558 |
scholar | rs1401880558 |
rs1401880558 | |
pharmgkb | rs1401880558 |
gwascentral | rs1401880558 |
openSNP | rs1401880558 |
23andMe | rs1401880558 |
SNPshot | rs1401880558 |
SNPdbe | rs1401880558 |
MSV3d | rs1401880558 |
GWAS Ctlg | rs1401880558 |
Max Magnitude | 3 |