rs369437262
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs369437262(C;C) |
Make rs369437262(C;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 23415228 |
Gene | MHRT, MYH7 |
is a | snp |
is | mentioned by |
dbSNP | rs369437262 |
dbSNP (classic) | rs369437262 |
ClinGen | rs369437262 |
ebi | rs369437262 |
HLI | rs369437262 |
Exac | rs369437262 |
Gnomad | rs369437262 |
Varsome | rs369437262 |
LitVar | rs369437262 |
Map | rs369437262 |
PheGenI | rs369437262 |
Biobank | rs369437262 |
1000 genomes | rs369437262 |
hgdp | rs369437262 |
ensembl | rs369437262 |
geneview | rs369437262 |
scholar | rs369437262 |
rs369437262 | |
pharmgkb | rs369437262 |
gwascentral | rs369437262 |
openSNP | rs369437262 |
23andMe | rs369437262 |
SNPshot | rs369437262 |
SNPdbe | rs369437262 |
MSV3d | rs369437262 |
GWAS Ctlg | rs369437262 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs369437262(C;C) |
Alt | rs369437262(C;C) |
Reference | Rs369437262(T;T) |
Significance | Probable-Pathogenic |
Disease | not specified Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy |
Variation | info |
Gene | MYH7 MHRT |
CLNDBN | not specified Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy |
Reversed | 0 |
HGVS | NC_000014.8:g.23884437T>C |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000154209.1, RCV000168915.2, RCV000462813.1, |