rs730880092
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs730880092(-;-) |
Make rs730880092(-;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 7583572 |
Gene | DSP |
is a | snp |
is | mentioned by |
dbSNP | rs730880092 |
dbSNP (classic) | rs730880092 |
ClinGen | rs730880092 |
ebi | rs730880092 |
HLI | rs730880092 |
Exac | rs730880092 |
Gnomad | rs730880092 |
Varsome | rs730880092 |
LitVar | rs730880092 |
Map | rs730880092 |
PheGenI | rs730880092 |
Biobank | rs730880092 |
1000 genomes | rs730880092 |
hgdp | rs730880092 |
ensembl | rs730880092 |
geneview | rs730880092 |
scholar | rs730880092 |
rs730880092 | |
pharmgkb | rs730880092 |
gwascentral | rs730880092 |
openSNP | rs730880092 |
23andMe | rs730880092 |
SNPshot | rs730880092 |
SNPdbe | rs730880092 |
MSV3d | rs730880092 |
GWAS Ctlg | rs730880092 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730880092(-;-) |
Alt | rs730880092(-;-) |
Reference | Rs730880092(A;A) |
Significance | Probable-Pathogenic |
Disease | Cardiomyopathy |
Variation | info |
Gene | DSP |
CLNDBN | Cardiomyopathy |
Reversed | 0 |
HGVS | NC_000006.11:g.7583805delA |
CLNSRC | |
CLNACC | RCV000157216.2, |