rs121913006
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121913006(A;A) |
Make rs121913006(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 31519867 |
Gene | DSG2 |
is a | snp |
is | mentioned by |
dbSNP | rs121913006 |
dbSNP (classic) | rs121913006 |
ClinGen | rs121913006 |
ebi | rs121913006 |
HLI | rs121913006 |
Exac | rs121913006 |
Gnomad | rs121913006 |
Varsome | rs121913006 |
LitVar | rs121913006 |
Map | rs121913006 |
PheGenI | rs121913006 |
Biobank | rs121913006 |
1000 genomes | rs121913006 |
hgdp | rs121913006 |
ensembl | rs121913006 |
geneview | rs121913006 |
scholar | rs121913006 |
rs121913006 | |
pharmgkb | rs121913006 |
gwascentral | rs121913006 |
openSNP | rs121913006 |
23andMe | rs121913006 |
SNPshot | rs121913006 |
SNPdbe | rs121913006 |
MSV3d | rs121913006 |
GWAS Ctlg | rs121913006 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913006(A;A) |
Alt | rs121913006(A;A) |
Reference | Rs121913006(G;G) |
Significance | Pathogenic |
Disease | Arrhythmogenic right ventricular cardiomyopathy not provided Arrhythmogenic right ventricular cardiomyopathy |
Variation | info |
Gene | DSG2 |
CLNDBN | Arrhythmogenic right ventricular cardiomyopathy, type 10 not provided Arrhythmogenic right ventricular cardiomyopathy |
Reversed | 0 |
HGVS | NC_000018.9:g.29099830G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000018303.29, RCV000181198.3, RCV000211715.1, |