rs773851192
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;T) | 3 | Carrier of a DFNB7/11 deafness mutation |
(G;G) | 0 | common/normal |
Make rs773851192(C;C) |
Make rs773851192(C;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 72789302 |
Gene | TMC1 |
is a | snp |
is | mentioned by |
dbSNP | rs773851192 |
dbSNP (classic) | rs773851192 |
ClinGen | rs773851192 |
ebi | rs773851192 |
HLI | rs773851192 |
Exac | rs773851192 |
Gnomad | rs773851192 |
Varsome | rs773851192 |
LitVar | rs773851192 |
Map | rs773851192 |
PheGenI | rs773851192 |
Biobank | rs773851192 |
1000 genomes | rs773851192 |
hgdp | rs773851192 |
ensembl | rs773851192 |
geneview | rs773851192 |
scholar | rs773851192 |
rs773851192 | |
pharmgkb | rs773851192 |
gwascentral | rs773851192 |
openSNP | rs773851192 |
23andMe | rs773851192 |
SNPshot | rs773851192 |
SNPdbe | rs773851192 |
MSV3d | rs773851192 |
GWAS Ctlg | rs773851192 |
Max Magnitude | 3 |