rs199560971
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 3 | Carrier of a DFNB7/11 deafness mutation |
(G;G) | 0 | common/normal |
Make rs199560971(A;A) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 72751859 |
Gene | TMC1 |
is a | snp |
is | mentioned by |
dbSNP | rs199560971 |
dbSNP (classic) | rs199560971 |
ClinGen | rs199560971 |
ebi | rs199560971 |
HLI | rs199560971 |
Exac | rs199560971 |
Gnomad | rs199560971 |
Varsome | rs199560971 |
LitVar | rs199560971 |
Map | rs199560971 |
PheGenI | rs199560971 |
Biobank | rs199560971 |
1000 genomes | rs199560971 |
hgdp | rs199560971 |
ensembl | rs199560971 |
geneview | rs199560971 |
scholar | rs199560971 |
rs199560971 | |
pharmgkb | rs199560971 |
gwascentral | rs199560971 |
openSNP | rs199560971 |
23andMe | rs199560971 |
SNPshot | rs199560971 |
SNPdbe | rs199560971 |
MSV3d | rs199560971 |
GWAS Ctlg | rs199560971 |
Max Magnitude | 3 |