rs193922410
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs193922410(A;G) |
Make rs193922410(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 63062248 |
Gene | TPM1 |
is a | snp |
is | mentioned by |
dbSNP | rs193922410 |
dbSNP (classic) | rs193922410 |
ClinGen | rs193922410 |
ebi | rs193922410 |
HLI | rs193922410 |
Exac | rs193922410 |
Gnomad | rs193922410 |
Varsome | rs193922410 |
LitVar | rs193922410 |
Map | rs193922410 |
PheGenI | rs193922410 |
Biobank | rs193922410 |
1000 genomes | rs193922410 |
hgdp | rs193922410 |
ensembl | rs193922410 |
geneview | rs193922410 |
scholar | rs193922410 |
rs193922410 | |
pharmgkb | rs193922410 |
gwascentral | rs193922410 |
openSNP | rs193922410 |
23andMe | rs193922410 |
SNPshot | rs193922410 |
SNPdbe | rs193922410 |
MSV3d | rs193922410 |
GWAS Ctlg | rs193922410 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs193922410(G;G) |
Alt | rs193922410(G;G) |
Reference | Rs193922410(A;A) |
Significance | Probable-Pathogenic |
Disease | Primary familial hypertrophic cardiomyopathy not specified |
Variation | info |
Gene | TPM1 |
CLNDBN | Primary familial hypertrophic cardiomyopathy not specified |
Reversed | 0 |
HGVS | NC_000015.9:g.63354447A>G |
CLNSRC | ClinVar LabCorp |
CLNACC | RCV000030569.1, RCV000159379.1, |