rs759242559
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs759242559(-;-) |
Make rs759242559(-;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 229432345 |
Gene | ACTA1 |
is a | snp |
is | mentioned by |
dbSNP | rs759242559 |
dbSNP (classic) | rs759242559 |
ClinGen | rs759242559 |
ebi | rs759242559 |
HLI | rs759242559 |
Exac | rs759242559 |
Gnomad | rs759242559 |
Varsome | rs759242559 |
LitVar | rs759242559 |
Map | rs759242559 |
PheGenI | rs759242559 |
Biobank | rs759242559 |
1000 genomes | rs759242559 |
hgdp | rs759242559 |
ensembl | rs759242559 |
geneview | rs759242559 |
scholar | rs759242559 |
rs759242559 | |
pharmgkb | rs759242559 |
gwascentral | rs759242559 |
openSNP | rs759242559 |
23andMe | rs759242559 |
SNPshot | rs759242559 |
SNPdbe | rs759242559 |
MSV3d | rs759242559 |
GWAS Ctlg | rs759242559 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759242559(-;-) |
Alt | rs759242559(-;-) |
Reference | Rs759242559(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACTA1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.229568092delC |
CLNSRC | |
CLNACC | RCV000479633.1, |