rs876661394
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 6.2 | Familial Hypertrophic Cardiomyopathy |
Make rs876661394(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 55154056 |
Gene | TNNI3 |
is a | snp |
is | mentioned by |
dbSNP | rs876661394 |
dbSNP (classic) | rs876661394 |
ClinGen | rs876661394 |
ebi | rs876661394 |
HLI | rs876661394 |
Exac | rs876661394 |
Gnomad | rs876661394 |
Varsome | rs876661394 |
LitVar | rs876661394 |
Map | rs876661394 |
PheGenI | rs876661394 |
Biobank | rs876661394 |
1000 genomes | rs876661394 |
hgdp | rs876661394 |
ensembl | rs876661394 |
geneview | rs876661394 |
scholar | rs876661394 |
rs876661394 | |
pharmgkb | rs876661394 |
gwascentral | rs876661394 |
openSNP | rs876661394 |
23andMe | rs876661394 |
SNPshot | rs876661394 |
SNPdbe | rs876661394 |
MSV3d | rs876661394 |
GWAS Ctlg | rs876661394 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876661394(T;T) |
Alt | rs876661394(T;T) |
Reference | Rs876661394(C;C) |
Significance | Pathogenic |
Disease | not provided Cardiovascular phenotype |
Variation | info |
Gene | TNNI3 |
CLNDBN | not provided Cardiovascular phenotype |
Reversed | 1 |
HGVS | NC_000019.9:g.55665424G>A |
CLNSRC | |
CLNACC | RCV000223834.1, RCV000248954.1, |