rs764817683
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;G) | 6.7 | Arrhythmogenic right ventricular dysplasia |
(G;G) | 0 | common in clinvar |
Make rs764817683(-;-) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 32821488 |
Gene | PKP2 |
is a | snp |
is | mentioned by |
dbSNP | rs764817683 |
dbSNP (classic) | rs764817683 |
ClinGen | rs764817683 |
ebi | rs764817683 |
HLI | rs764817683 |
Exac | rs764817683 |
Gnomad | rs764817683 |
Varsome | rs764817683 |
LitVar | rs764817683 |
Map | rs764817683 |
PheGenI | rs764817683 |
Biobank | rs764817683 |
1000 genomes | rs764817683 |
hgdp | rs764817683 |
ensembl | rs764817683 |
geneview | rs764817683 |
scholar | rs764817683 |
rs764817683 | |
pharmgkb | rs764817683 |
gwascentral | rs764817683 |
openSNP | rs764817683 |
23andMe | rs764817683 |
SNPshot | rs764817683 |
SNPdbe | rs764817683 |
MSV3d | rs764817683 |
GWAS Ctlg | rs764817683 |
Max Magnitude | 6.7 |
ClinVar | |
---|---|
Risk | rs764817683(-;-) |
Alt | rs764817683(-;-) |
Reference | Rs764817683(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PKP2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.32974422delG |
CLNSRC | |
CLNACC | RCV000183795.2, |