rs794728228
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 6.5 | Familial thoracic aortic aneurysms and dissections (FTAAD) |
Make rs794728228(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 48468064 |
Gene | FBN1 |
is a | snp |
is | mentioned by |
dbSNP | rs794728228 |
dbSNP (classic) | rs794728228 |
ClinGen | rs794728228 |
ebi | rs794728228 |
HLI | rs794728228 |
Exac | rs794728228 |
Gnomad | rs794728228 |
Varsome | rs794728228 |
LitVar | rs794728228 |
Map | rs794728228 |
PheGenI | rs794728228 |
Biobank | rs794728228 |
1000 genomes | rs794728228 |
hgdp | rs794728228 |
ensembl | rs794728228 |
geneview | rs794728228 |
scholar | rs794728228 |
rs794728228 | |
pharmgkb | rs794728228 |
gwascentral | rs794728228 |
openSNP | rs794728228 |
23andMe | rs794728228 |
SNPshot | rs794728228 |
SNPdbe | rs794728228 |
MSV3d | rs794728228 |
GWAS Ctlg | rs794728228 |
Max Magnitude | 6.5 |
ClinVar | |
---|---|
Risk | rs794728228(T;T) |
Alt | rs794728228(T;T) |
Reference | Rs794728228(C;C) |
Significance | Pathogenic |
Disease | not provided Marfan syndrome |
Variation | info |
Gene | FBN1 |
CLNDBN | not provided Marfan syndrome |
Reversed | 1 |
HGVS | NC_000015.9:g.48760261G>A |
CLNSRC | |
CLNACC | RCV000181529.3, RCV000462664.1, |