rs66785829
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs66785829(A;A) |
Make rs66785829(A;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 113365051 |
Gene | ANK2 |
is a | snp |
is | mentioned by |
dbSNP | rs66785829 |
dbSNP (classic) | rs66785829 |
ClinGen | rs66785829 |
ebi | rs66785829 |
HLI | rs66785829 |
Exac | rs66785829 |
Gnomad | rs66785829 |
Varsome | rs66785829 |
LitVar | rs66785829 |
Map | rs66785829 |
PheGenI | rs66785829 |
Biobank | rs66785829 |
1000 genomes | rs66785829 |
hgdp | rs66785829 |
ensembl | rs66785829 |
geneview | rs66785829 |
scholar | rs66785829 |
rs66785829 | |
pharmgkb | rs66785829 |
gwascentral | rs66785829 |
openSNP | rs66785829 |
23andMe | rs66785829 |
SNPshot | rs66785829 |
SNPdbe | rs66785829 |
MSV3d | rs66785829 |
GWAS Ctlg | rs66785829 |
Merged from | Rs66785830 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs66785829(A;A) rs66785829(C;C) |
Alt | rs66785829(A;A) rs66785829(C;C) |
Reference | Rs66785829(T;T) |
Significance | Probable-non-pathogenic |
Disease | Arrhythmia Long QT syndrome Cardiac arrhythmia not specified |
Variation | info |
Gene | ANK2 |
CLNDBN | Arrhythmia Long QT syndrome Cardiac arrhythmia not specified |
Reversed | 0 |
HGVS | NC_000004.11:g.114286207T>A |
CLNSRC | Cardiovascular Biomedical Research Unit ClinVar GeneDx |
CLNACC | RCV000058344.3, RCV000168225.3, RCV000171748.3, RCV000211889.1, |