rs730881061
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs730881061(A;G) |
Make rs730881061(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 52451415 |
Gene | TNNC1 |
is a | snp |
is | mentioned by |
dbSNP | rs730881061 |
dbSNP (classic) | rs730881061 |
ClinGen | rs730881061 |
ebi | rs730881061 |
HLI | rs730881061 |
Exac | rs730881061 |
Gnomad | rs730881061 |
Varsome | rs730881061 |
LitVar | rs730881061 |
Map | rs730881061 |
PheGenI | rs730881061 |
Biobank | rs730881061 |
1000 genomes | rs730881061 |
hgdp | rs730881061 |
ensembl | rs730881061 |
geneview | rs730881061 |
scholar | rs730881061 |
rs730881061 | |
pharmgkb | rs730881061 |
gwascentral | rs730881061 |
openSNP | rs730881061 |
23andMe | rs730881061 |
SNPshot | rs730881061 |
SNPdbe | rs730881061 |
MSV3d | rs730881061 |
GWAS Ctlg | rs730881061 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730881061(G;G) |
Alt | rs730881061(G;G) |
Reference | Rs730881061(A;A) |
Significance | Probable-Pathogenic |
Disease | not specified Dilated cardiomyopathy 1Z Familial hypertrophic cardiomyopathy 13 |
Variation | info |
Gene | TNNC1 |
CLNDBN | not specified Dilated cardiomyopathy 1Z Familial hypertrophic cardiomyopathy 13 |
Reversed | 1 |
HGVS | NC_000003.11:g.52485431T>C |
CLNSRC | |
CLNACC | RCV000159200.2, RCV000471611.1, |