rs193922409
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs193922409(A;A) |
Make rs193922409(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 55151905 |
Gene | TNNI3 |
is a | snp |
is | mentioned by |
dbSNP | rs193922409 |
dbSNP (classic) | rs193922409 |
ClinGen | rs193922409 |
ebi | rs193922409 |
HLI | rs193922409 |
Exac | rs193922409 |
Gnomad | rs193922409 |
Varsome | rs193922409 |
LitVar | rs193922409 |
Map | rs193922409 |
PheGenI | rs193922409 |
Biobank | rs193922409 |
1000 genomes | rs193922409 |
hgdp | rs193922409 |
ensembl | rs193922409 |
geneview | rs193922409 |
scholar | rs193922409 |
rs193922409 | |
pharmgkb | rs193922409 |
gwascentral | rs193922409 |
openSNP | rs193922409 |
23andMe | rs193922409 |
SNPshot | rs193922409 |
SNPdbe | rs193922409 |
MSV3d | rs193922409 |
GWAS Ctlg | rs193922409 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs193922409(A;A) rs193922409(T;T) |
Alt | rs193922409(A;A) rs193922409(T;T) |
Reference | Rs193922409(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified Primary familial hypertrophic cardiomyopathy not provided |
Variation | info |
Gene | TNNI3 |
CLNDBN | not specified Primary familial hypertrophic cardiomyopathy not provided |
Reversed | 1 |
HGVS | NC_000019.9:g.55663273C>A; NC_000019.9:g.55663273C>T |
CLNSRC | ClinVar LabCorp |
CLNACC | RCV000159241.1, RCV000030565.1, RCV000159240.2, |