rs730881158
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs730881158(A;G) |
Make rs730881158(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 15 |
Position | 63057037 |
Gene | TPM1 |
is a | snp |
is | mentioned by |
dbSNP | rs730881158 |
dbSNP (classic) | rs730881158 |
ClinGen | rs730881158 |
ebi | rs730881158 |
HLI | rs730881158 |
Exac | rs730881158 |
Gnomad | rs730881158 |
Varsome | rs730881158 |
LitVar | rs730881158 |
Map | rs730881158 |
PheGenI | rs730881158 |
Biobank | rs730881158 |
1000 genomes | rs730881158 |
hgdp | rs730881158 |
ensembl | rs730881158 |
geneview | rs730881158 |
scholar | rs730881158 |
rs730881158 | |
pharmgkb | rs730881158 |
gwascentral | rs730881158 |
openSNP | rs730881158 |
23andMe | rs730881158 |
SNPshot | rs730881158 |
SNPdbe | rs730881158 |
MSV3d | rs730881158 |
GWAS Ctlg | rs730881158 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730881158(G;G) |
Alt | rs730881158(G;G) |
Reference | Rs730881158(A;A) |
Significance | Probable-Pathogenic |
Disease | Cardiomyopathy |
Variation | info |
Gene | TPM1 |
CLNDBN | Cardiomyopathy |
Reversed | 0 |
HGVS | NC_000015.9:g.63349236A>G |
CLNSRC | |
CLNACC | RCV000159409.1, |