rs373520843
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs373520843(A;A) |
Make rs373520843(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 18162639 |
Gene | MYO15A |
is a | snp |
is | mentioned by |
dbSNP | rs373520843 |
dbSNP (classic) | rs373520843 |
ClinGen | rs373520843 |
ebi | rs373520843 |
HLI | rs373520843 |
Exac | rs373520843 |
Gnomad | rs373520843 |
Varsome | rs373520843 |
LitVar | rs373520843 |
Map | rs373520843 |
PheGenI | rs373520843 |
Biobank | rs373520843 |
1000 genomes | rs373520843 |
hgdp | rs373520843 |
ensembl | rs373520843 |
geneview | rs373520843 |
scholar | rs373520843 |
rs373520843 | |
pharmgkb | rs373520843 |
gwascentral | rs373520843 |
openSNP | rs373520843 |
23andMe | rs373520843 |
SNPshot | rs373520843 |
SNPdbe | rs373520843 |
MSV3d | rs373520843 |
GWAS Ctlg | rs373520843 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs373520843(A;A) |
Alt | rs373520843(A;A) |
Reference | Rs373520843(G;G) |
Significance | Pathogenic |
Disease | Deafness |
Variation | info |
Gene | MYO15A |
CLNDBN | Deafness, autosomal recessive 3 |
Reversed | 0 |
HGVS | NC_000017.10:g.18065953G>A |
CLNSRC | |
CLNACC | RCV000454294.1, |