rs28932774
From SNPedia
Merged into | rs104894370 |
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 3 | Familial Hypertrophic Cardiomyopathy |
(C;T) | 3 | Familial Hypertrophic Cardiomyopathy |
(T;T) | 0 |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 110919145 |
Gene | MYL2 |
is a | snp |
is | mentioned by |
dbSNP | rs28932774 |
dbSNP (classic) | rs28932774 |
ClinGen | rs28932774 |
ebi | rs28932774 |
HLI | rs28932774 |
Exac | rs28932774 |
Gnomad | rs28932774 |
Varsome | rs28932774 |
LitVar | rs28932774 |
Map | rs28932774 |
PheGenI | rs28932774 |
Biobank | rs28932774 |
1000 genomes | rs28932774 |
hgdp | rs28932774 |
ensembl | rs28932774 |
geneview | rs28932774 |
scholar | rs28932774 |
rs28932774 | |
pharmgkb | rs28932774 |
gwascentral | rs28932774 |
openSNP | rs28932774 |
23andMe | rs28932774 |
SNPshot | rs28932774 |
SNPdbe | rs28932774 |
MSV3d | rs28932774 |
GWAS Ctlg | rs28932774 |
Status | Merged into rs104894370 |
Max Magnitude | 3 |
Familial hypertrophic cardiomyopathy
see also OMIM 160781.0005
Note: this SNP, rs28932774, appears to tag the same polymorphism as rs104894370