rs397515325
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs397515325(A;G) |
Make rs397515325(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 88947371 |
Gene | ACTA2 |
is a | snp |
is | mentioned by |
dbSNP | rs397515325 |
dbSNP (classic) | rs397515325 |
ClinGen | rs397515325 |
ebi | rs397515325 |
HLI | rs397515325 |
Exac | rs397515325 |
Gnomad | rs397515325 |
Varsome | rs397515325 |
LitVar | rs397515325 |
Map | rs397515325 |
PheGenI | rs397515325 |
Biobank | rs397515325 |
1000 genomes | rs397515325 |
hgdp | rs397515325 |
ensembl | rs397515325 |
geneview | rs397515325 |
scholar | rs397515325 |
rs397515325 | |
pharmgkb | rs397515325 |
gwascentral | rs397515325 |
openSNP | rs397515325 |
23andMe | rs397515325 |
SNPshot | rs397515325 |
SNPdbe | rs397515325 |
MSV3d | rs397515325 |
GWAS Ctlg | rs397515325 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397515325(G;G) |
Alt | rs397515325(G;G) |
Reference | Rs397515325(A;A) |
Significance | Pathogenic |
Disease | Aortic aneurysm |
Variation | info |
Gene | ACTA2 STAMBPL1 |
CLNDBN | Aortic aneurysm, familial thoracic 6 |
Reversed | 1 |
HGVS | NC_000010.10:g.90707128T>C |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000055648.26, |