rs749491943
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;T) | 3 | Carrier of a DFNB7/11 deafness mutation |
(T;T) | 0 | common/normal |
Make rs749491943(A;A) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 72789234 |
Gene | TMC1 |
is a | snp |
is | mentioned by |
dbSNP | rs749491943 |
dbSNP (classic) | rs749491943 |
ClinGen | rs749491943 |
ebi | rs749491943 |
HLI | rs749491943 |
Exac | rs749491943 |
Gnomad | rs749491943 |
Varsome | rs749491943 |
LitVar | rs749491943 |
Map | rs749491943 |
PheGenI | rs749491943 |
Biobank | rs749491943 |
1000 genomes | rs749491943 |
hgdp | rs749491943 |
ensembl | rs749491943 |
geneview | rs749491943 |
scholar | rs749491943 |
rs749491943 | |
pharmgkb | rs749491943 |
gwascentral | rs749491943 |
openSNP | rs749491943 |
23andMe | rs749491943 |
SNPshot | rs749491943 |
SNPdbe | rs749491943 |
MSV3d | rs749491943 |
GWAS Ctlg | rs749491943 |
Max Magnitude | 3 |