rs1169090943
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common/normal |
(G;T) | 3 | Carrier of a DFNB7/11 deafness mutation |
Make rs1169090943(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 72648665 |
Gene | TMC1 |
is a | snp |
is | mentioned by |
dbSNP | rs1169090943 |
dbSNP (classic) | rs1169090943 |
ClinGen | rs1169090943 |
ebi | rs1169090943 |
HLI | rs1169090943 |
Exac | rs1169090943 |
Gnomad | rs1169090943 |
Varsome | rs1169090943 |
LitVar | rs1169090943 |
Map | rs1169090943 |
PheGenI | rs1169090943 |
Biobank | rs1169090943 |
1000 genomes | rs1169090943 |
hgdp | rs1169090943 |
ensembl | rs1169090943 |
geneview | rs1169090943 |
scholar | rs1169090943 |
rs1169090943 | |
pharmgkb | rs1169090943 |
gwascentral | rs1169090943 |
openSNP | rs1169090943 |
23andMe | rs1169090943 |
SNPshot | rs1169090943 |
SNPdbe | rs1169090943 |
MSV3d | rs1169090943 |
GWAS Ctlg | rs1169090943 |
Max Magnitude | 3 |