rs1290684098
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;C) | 3 | Carrier of a DFNB7/11 deafness mutation |
(C;C) | 0 | common/normal |
Make rs1290684098(C;T) |
Make rs1290684098(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 72820866 |
Gene | TMC1 |
is a | snp |
is | mentioned by |
dbSNP | rs1290684098 |
dbSNP (classic) | rs1290684098 |
ClinGen | rs1290684098 |
ebi | rs1290684098 |
HLI | rs1290684098 |
Exac | rs1290684098 |
Gnomad | rs1290684098 |
Varsome | rs1290684098 |
LitVar | rs1290684098 |
Map | rs1290684098 |
PheGenI | rs1290684098 |
Biobank | rs1290684098 |
1000 genomes | rs1290684098 |
hgdp | rs1290684098 |
ensembl | rs1290684098 |
geneview | rs1290684098 |
scholar | rs1290684098 |
rs1290684098 | |
pharmgkb | rs1290684098 |
gwascentral | rs1290684098 |
openSNP | rs1290684098 |
23andMe | rs1290684098 |
SNPshot | rs1290684098 |
SNPdbe | rs1290684098 |
MSV3d | rs1290684098 |
GWAS Ctlg | rs1290684098 |
Max Magnitude | 3 |