rs193922667
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs193922667(A;A) |
Make rs193922667(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 19186265 |
Gene | CSRP3 |
is a | snp |
is | mentioned by |
dbSNP | rs193922667 |
dbSNP (classic) | rs193922667 |
ClinGen | rs193922667 |
ebi | rs193922667 |
HLI | rs193922667 |
Exac | rs193922667 |
Gnomad | rs193922667 |
Varsome | rs193922667 |
LitVar | rs193922667 |
Map | rs193922667 |
PheGenI | rs193922667 |
Biobank | rs193922667 |
1000 genomes | rs193922667 |
hgdp | rs193922667 |
ensembl | rs193922667 |
geneview | rs193922667 |
scholar | rs193922667 |
rs193922667 | |
pharmgkb | rs193922667 |
gwascentral | rs193922667 |
openSNP | rs193922667 |
23andMe | rs193922667 |
SNPshot | rs193922667 |
SNPdbe | rs193922667 |
MSV3d | rs193922667 |
GWAS Ctlg | rs193922667 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs193922667(A;A) |
Alt | rs193922667(A;A) |
Reference | Rs193922667(G;G) |
Significance | Probable-Pathogenic |
Disease | Cardiomyopathy |
Variation | info |
Gene | CSRP3 |
CLNDBN | Cardiomyopathy |
Reversed | 1 |
HGVS | NC_000011.9:g.19207812C>T |
CLNSRC | ClinVar LabCorp |
CLNACC | RCV000029622.1, |