rs587777134
From SNPedia
Orientation | plus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(T;T) | 0 | common in clinvar |
Make rs587777134(A;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 67606868 |
Gene | CTNNA3 |
is a | snp |
is | mentioned by |
dbSNP | rs587777134 |
dbSNP (classic) | rs587777134 |
ClinGen | rs587777134 |
ebi | rs587777134 |
HLI | rs587777134 |
Exac | rs587777134 |
Gnomad | rs587777134 |
Varsome | rs587777134 |
LitVar | rs587777134 |
Map | rs587777134 |
PheGenI | rs587777134 |
Biobank | rs587777134 |
1000 genomes | rs587777134 |
hgdp | rs587777134 |
ensembl | rs587777134 |
geneview | rs587777134 |
scholar | rs587777134 |
rs587777134 | |
pharmgkb | rs587777134 |
gwascentral | rs587777134 |
openSNP | rs587777134 |
23andMe | rs587777134 |
SNPshot | rs587777134 |
SNPdbe | rs587777134 |
MSV3d | rs587777134 |
GWAS Ctlg | rs587777134 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | Rs587777134(A;A) |
Alt | Rs587777134(A;A) |
Reference | Rs587777134(T;T) |
Significance | Pathogenic |
Disease | Arrhythmogenic right ventricular dysplasia |
Variation | info |
Gene | CTNNA3 |
CLNDBN | Arrhythmogenic right ventricular dysplasia, familial, 13 |
Reversed | 1 |
HGVS | NC_000010.10:g.69366626A>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000087056.3, |