rs606231315
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs606231315(C;T) |
Make rs606231315(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 23431678 |
Gene | MYH7 |
is a | snp |
is | mentioned by |
dbSNP | rs606231315 |
dbSNP (classic) | rs606231315 |
ClinGen | rs606231315 |
ebi | rs606231315 |
HLI | rs606231315 |
Exac | rs606231315 |
Gnomad | rs606231315 |
Varsome | rs606231315 |
LitVar | rs606231315 |
Map | rs606231315 |
PheGenI | rs606231315 |
Biobank | rs606231315 |
1000 genomes | rs606231315 |
hgdp | rs606231315 |
ensembl | rs606231315 |
geneview | rs606231315 |
scholar | rs606231315 |
rs606231315 | |
pharmgkb | rs606231315 |
gwascentral | rs606231315 |
openSNP | rs606231315 |
23andMe | rs606231315 |
SNPshot | rs606231315 |
SNPdbe | rs606231315 |
MSV3d | rs606231315 |
GWAS Ctlg | rs606231315 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs606231315(T;T) |
Alt | rs606231315(T;T) |
Reference | Rs606231315(C;C) |
Significance | Probable-Pathogenic |
Disease | Familial cardiomyopathy |
Variation | info |
Gene | MYH7 |
CLNDBN | Familial cardiomyopathy |
Reversed | 0 |
HGVS | NC_000014.8:g.23900887C>T |
CLNSRC | |
CLNACC | RCV000148983.1, |