rs756960425
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common/normal |
(A;T) | 3 | Carrier of a DFNB7/11 deafness mutation |
Make rs756960425(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 72751910 |
Gene | TMC1 |
is a | snp |
is | mentioned by |
dbSNP | rs756960425 |
dbSNP (classic) | rs756960425 |
ClinGen | rs756960425 |
ebi | rs756960425 |
HLI | rs756960425 |
Exac | rs756960425 |
Gnomad | rs756960425 |
Varsome | rs756960425 |
LitVar | rs756960425 |
Map | rs756960425 |
PheGenI | rs756960425 |
Biobank | rs756960425 |
1000 genomes | rs756960425 |
hgdp | rs756960425 |
ensembl | rs756960425 |
geneview | rs756960425 |
scholar | rs756960425 |
rs756960425 | |
pharmgkb | rs756960425 |
gwascentral | rs756960425 |
openSNP | rs756960425 |
23andMe | rs756960425 |
SNPshot | rs756960425 |
SNPdbe | rs756960425 |
MSV3d | rs756960425 |
GWAS Ctlg | rs756960425 |
Max Magnitude | 3 |