rs119103279
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs119103279(A;A) |
Make rs119103279(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 50210385 |
Gene | MYH14 |
is a | snp |
is | mentioned by |
dbSNP | rs119103279 |
dbSNP (classic) | rs119103279 |
ClinGen | rs119103279 |
ebi | rs119103279 |
HLI | rs119103279 |
Exac | rs119103279 |
Gnomad | rs119103279 |
Varsome | rs119103279 |
LitVar | rs119103279 |
Map | rs119103279 |
PheGenI | rs119103279 |
Biobank | rs119103279 |
1000 genomes | rs119103279 |
hgdp | rs119103279 |
ensembl | rs119103279 |
geneview | rs119103279 |
scholar | rs119103279 |
rs119103279 | |
pharmgkb | rs119103279 |
gwascentral | rs119103279 |
openSNP | rs119103279 |
23andMe | rs119103279 |
SNPshot | rs119103279 |
SNPdbe | rs119103279 |
MSV3d | rs119103279 |
GWAS Ctlg | rs119103279 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs119103279(A;A) |
Alt | rs119103279(A;A) |
Reference | Rs119103279(C;C) |
Significance | Pathogenic |
Disease | Deafness |
Variation | info |
Gene | MYH14 |
CLNDBN | Deafness, autosomal dominant 4 |
Reversed | 0 |
HGVS | NC_000019.9:g.50713642C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000002280.3, |