rs200171616
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;T) | 3 | Carrier of a DFNB7/11 deafness mutation |
Make rs200171616(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 72792320 |
Gene | TMC1 |
is a | snp |
is | mentioned by |
dbSNP | rs200171616 |
dbSNP (classic) | rs200171616 |
ClinGen | rs200171616 |
ebi | rs200171616 |
HLI | rs200171616 |
Exac | rs200171616 |
Gnomad | rs200171616 |
Varsome | rs200171616 |
LitVar | rs200171616 |
Map | rs200171616 |
PheGenI | rs200171616 |
Biobank | rs200171616 |
1000 genomes | rs200171616 |
hgdp | rs200171616 |
ensembl | rs200171616 |
geneview | rs200171616 |
scholar | rs200171616 |
rs200171616 | |
pharmgkb | rs200171616 |
gwascentral | rs200171616 |
openSNP | rs200171616 |
23andMe | rs200171616 |
SNPshot | rs200171616 |
SNPdbe | rs200171616 |
MSV3d | rs200171616 |
GWAS Ctlg | rs200171616 |
Max Magnitude | 3 |