rs142534126
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs142534126(C;T) |
Make rs142534126(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 113345961 |
Gene | ANK2 |
is a | snp |
is | mentioned by |
dbSNP | rs142534126 |
dbSNP (classic) | rs142534126 |
ClinGen | rs142534126 |
ebi | rs142534126 |
HLI | rs142534126 |
Exac | rs142534126 |
Gnomad | rs142534126 |
Varsome | rs142534126 |
LitVar | rs142534126 |
Map | rs142534126 |
PheGenI | rs142534126 |
Biobank | rs142534126 |
1000 genomes | rs142534126 |
hgdp | rs142534126 |
ensembl | rs142534126 |
geneview | rs142534126 |
scholar | rs142534126 |
rs142534126 | |
pharmgkb | rs142534126 |
gwascentral | rs142534126 |
openSNP | rs142534126 |
23andMe | rs142534126 |
SNPshot | rs142534126 |
SNPdbe | rs142534126 |
MSV3d | rs142534126 |
GWAS Ctlg | rs142534126 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs142534126(T;T) |
Alt | rs142534126(T;T) |
Reference | Rs142534126(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided Cardiovascular phenotype |
Variation | info |
Gene | ANK2 |
CLNDBN | not provided Cardiovascular phenotype |
Reversed | 0 |
HGVS | NC_000004.11:g.114267117C>T |
CLNSRC | |
CLNACC | RCV000170701.3, RCV000250831.1, |