rs757327146
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;G) | 3 | Carrier of a DFNB7/11 deafness mutation |
Make rs757327146(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 72789236 |
Gene | TMC1 |
is a | snp |
is | mentioned by |
dbSNP | rs757327146 |
dbSNP (classic) | rs757327146 |
ClinGen | rs757327146 |
ebi | rs757327146 |
HLI | rs757327146 |
Exac | rs757327146 |
Gnomad | rs757327146 |
Varsome | rs757327146 |
LitVar | rs757327146 |
Map | rs757327146 |
PheGenI | rs757327146 |
Biobank | rs757327146 |
1000 genomes | rs757327146 |
hgdp | rs757327146 |
ensembl | rs757327146 |
geneview | rs757327146 |
scholar | rs757327146 |
rs757327146 | |
pharmgkb | rs757327146 |
gwascentral | rs757327146 |
openSNP | rs757327146 |
23andMe | rs757327146 |
SNPshot | rs757327146 |
SNPdbe | rs757327146 |
MSV3d | rs757327146 |
GWAS Ctlg | rs757327146 |
Max Magnitude | 3 |