rs587777928
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587777928(-;T) |
Make rs587777928(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 155710653 |
Gene | GUCY1A3 |
is a | snp |
is | mentioned by |
dbSNP | rs587777928 |
dbSNP (classic) | rs587777928 |
ClinGen | rs587777928 |
ebi | rs587777928 |
HLI | rs587777928 |
Exac | rs587777928 |
Gnomad | rs587777928 |
Varsome | rs587777928 |
LitVar | rs587777928 |
Map | rs587777928 |
PheGenI | rs587777928 |
Biobank | rs587777928 |
1000 genomes | rs587777928 |
hgdp | rs587777928 |
ensembl | rs587777928 |
geneview | rs587777928 |
scholar | rs587777928 |
rs587777928 | |
pharmgkb | rs587777928 |
gwascentral | rs587777928 |
openSNP | rs587777928 |
23andMe | rs587777928 |
SNPshot | rs587777928 |
SNPdbe | rs587777928 |
MSV3d | rs587777928 |
GWAS Ctlg | rs587777928 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777928(T;T) |
Alt | rs587777928(T;T) |
Reference | Rs587777928(-;-) |
Significance | Pathogenic |
Disease | Myocardial infarction 1 |
Variation | info |
Gene | GUCY1A3 |
CLNDBN | Myocardial infarction 1 |
Reversed | 0 |
HGVS | NC_000004.11:g.156631805dupT |
CLNSRC | |
CLNACC | RCV000077777.1, |