rs28933099
From SNPedia
Merged into | rs104894369 |
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 3 | Familial Hypertrophic Cardiomyopathy |
(A;G) | 3 | Familial Hypertrophic Cardiomyopathy |
(G;G) | 0 |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 110914287 |
Gene | MYL2 |
is a | snp |
is | mentioned by |
dbSNP | rs28933099 |
dbSNP (classic) | rs28933099 |
ClinGen | rs28933099 |
ebi | rs28933099 |
HLI | rs28933099 |
Exac | rs28933099 |
Gnomad | rs28933099 |
Varsome | rs28933099 |
LitVar | rs28933099 |
Map | rs28933099 |
PheGenI | rs28933099 |
Biobank | rs28933099 |
1000 genomes | rs28933099 |
hgdp | rs28933099 |
ensembl | rs28933099 |
geneview | rs28933099 |
scholar | rs28933099 |
rs28933099 | |
pharmgkb | rs28933099 |
gwascentral | rs28933099 |
openSNP | rs28933099 |
23andMe | rs28933099 |
SNPshot | rs28933099 |
SNPdbe | rs28933099 |
MSV3d | rs28933099 |
GWAS Ctlg | rs28933099 |
Status | Merged into rs104894369 |
Max Magnitude | 3 |
Familial hypertrophic cardiomyopathy
see also OMIM 160781.0004
Note: this SNP, rs28933099, appears to tag the same polymorphism as rs104894369