rs142019584
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs142019584(A;A) |
Make rs142019584(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 19182719 |
Gene | CSRP3 |
is a | snp |
is | mentioned by |
dbSNP | rs142019584 |
dbSNP (classic) | rs142019584 |
ClinGen | rs142019584 |
ebi | rs142019584 |
HLI | rs142019584 |
Exac | rs142019584 |
Gnomad | rs142019584 |
Varsome | rs142019584 |
LitVar | rs142019584 |
Map | rs142019584 |
PheGenI | rs142019584 |
Biobank | rs142019584 |
1000 genomes | rs142019584 |
hgdp | rs142019584 |
ensembl | rs142019584 |
geneview | rs142019584 |
scholar | rs142019584 |
rs142019584 | |
pharmgkb | rs142019584 |
gwascentral | rs142019584 |
openSNP | rs142019584 |
23andMe | rs142019584 |
SNPshot | rs142019584 |
SNPdbe | rs142019584 |
MSV3d | rs142019584 |
GWAS Ctlg | rs142019584 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs142019584(A;A) |
Alt | rs142019584(A;A) |
Reference | Rs142019584(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified Familial hypertrophic cardiomyopathy 12 Dilated cardiomyopathy 1M |
Variation | info |
Gene | CSRP3 |
CLNDBN | not specified Familial hypertrophic cardiomyopathy 12 Dilated cardiomyopathy 1M |
Reversed | 0 |
HGVS | NC_000011.9:g.19204266G>A |
CLNSRC | |
CLNACC | RCV000150366.1, RCV000201497.1, RCV000231901.1, |