rs193922668
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(ATT;ATT) | 0 | common in clinvar |
Make rs193922668(-;-) |
Make rs193922668(-;ATT) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 7568554 |
Gene | DSP |
is a | snp |
is | mentioned by |
dbSNP | rs193922668 |
dbSNP (classic) | rs193922668 |
ClinGen | rs193922668 |
ebi | rs193922668 |
HLI | rs193922668 |
Exac | rs193922668 |
Gnomad | rs193922668 |
Varsome | rs193922668 |
LitVar | rs193922668 |
Map | rs193922668 |
PheGenI | rs193922668 |
Biobank | rs193922668 |
1000 genomes | rs193922668 |
hgdp | rs193922668 |
ensembl | rs193922668 |
geneview | rs193922668 |
scholar | rs193922668 |
rs193922668 | |
pharmgkb | rs193922668 |
gwascentral | rs193922668 |
openSNP | rs193922668 |
23andMe | rs193922668 |
SNPshot | rs193922668 |
SNPdbe | rs193922668 |
MSV3d | rs193922668 |
GWAS Ctlg | rs193922668 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs193922668(-;-) |
Alt | rs193922668(-;-) |
Reference | Rs193922668(ATT;ATT) |
Significance | Probable-Pathogenic |
Disease | Cardiomyopathy |
Variation | info |
Gene | DSP |
CLNDBN | Cardiomyopathy |
Reversed | 0 |
HGVS | NC_000006.11:g.7568787_7568789delATT |
CLNSRC | ClinVar |
CLNACC | RCV000029676.1, |