rs398123562
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs398123562(G;T) |
Make rs398123562(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 229432877 |
Gene | ACTA1 |
is a | snp |
is | mentioned by |
dbSNP | rs398123562 |
dbSNP (classic) | rs398123562 |
ClinGen | rs398123562 |
ebi | rs398123562 |
HLI | rs398123562 |
Exac | rs398123562 |
Gnomad | rs398123562 |
Varsome | rs398123562 |
LitVar | rs398123562 |
Map | rs398123562 |
PheGenI | rs398123562 |
Biobank | rs398123562 |
1000 genomes | rs398123562 |
hgdp | rs398123562 |
ensembl | rs398123562 |
geneview | rs398123562 |
scholar | rs398123562 |
rs398123562 | |
pharmgkb | rs398123562 |
gwascentral | rs398123562 |
openSNP | rs398123562 |
23andMe | rs398123562 |
SNPshot | rs398123562 |
SNPdbe | rs398123562 |
MSV3d | rs398123562 |
GWAS Ctlg | rs398123562 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs398123562(T;T) |
Alt | rs398123562(T;T) |
Reference | Rs398123562(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACTA1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000001.10:g.229568624C>A |
CLNSRC | HGMD UniProtKB (protein) |
CLNACC | RCV000079464.4, |