rs1448901281
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;T) | 3 | Carrier of a DFNB7/11 deafness mutation |
(T;T) | 0 | common/normal |
Make rs1448901281(C;C) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 72826895 |
Gene | TMC1 |
is a | snp |
is | mentioned by |
dbSNP | rs1448901281 |
dbSNP (classic) | rs1448901281 |
ClinGen | rs1448901281 |
ebi | rs1448901281 |
HLI | rs1448901281 |
Exac | rs1448901281 |
Gnomad | rs1448901281 |
Varsome | rs1448901281 |
LitVar | rs1448901281 |
Map | rs1448901281 |
PheGenI | rs1448901281 |
Biobank | rs1448901281 |
1000 genomes | rs1448901281 |
hgdp | rs1448901281 |
ensembl | rs1448901281 |
geneview | rs1448901281 |
scholar | rs1448901281 |
rs1448901281 | |
pharmgkb | rs1448901281 |
gwascentral | rs1448901281 |
openSNP | rs1448901281 |
23andMe | rs1448901281 |
SNPshot | rs1448901281 |
SNPdbe | rs1448901281 |
MSV3d | rs1448901281 |
GWAS Ctlg | rs1448901281 |
Max Magnitude | 3 |