rs533568822
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs533568822(G;T) |
Make rs533568822(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 18 |
Position | 34882130 |
Gene | DTNA |
is a | snp |
is | mentioned by |
dbSNP | rs533568822 |
dbSNP (classic) | rs533568822 |
ClinGen | rs533568822 |
ebi | rs533568822 |
HLI | rs533568822 |
Exac | rs533568822 |
Gnomad | rs533568822 |
Varsome | rs533568822 |
LitVar | rs533568822 |
Map | rs533568822 |
PheGenI | rs533568822 |
Biobank | rs533568822 |
1000 genomes | rs533568822 |
hgdp | rs533568822 |
ensembl | rs533568822 |
geneview | rs533568822 |
scholar | rs533568822 |
rs533568822 | |
pharmgkb | rs533568822 |
gwascentral | rs533568822 |
openSNP | rs533568822 |
23andMe | rs533568822 |
SNPshot | rs533568822 |
SNPdbe | rs533568822 |
MSV3d | rs533568822 |
GWAS Ctlg | rs533568822 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs533568822(T;T) |
Alt | rs533568822(T;T) |
Reference | Rs533568822(G;G) |
Significance | Probable-Pathogenic |
Disease | Ménière's disease |
Variation | info |
Gene | DTNA |
CLNDBN | Ménière's disease |
Reversed | 0 |
HGVS | NC_000018.9:g.32462094G>T |
CLNSRC | |
CLNACC | RCV000149520.1, |