rs536588176
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs536588176(C;T) |
Make rs536588176(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 48520715 |
Gene | FBN1 |
is a | snp |
is | mentioned by |
dbSNP | rs536588176 |
dbSNP (classic) | rs536588176 |
ClinGen | rs536588176 |
ebi | rs536588176 |
HLI | rs536588176 |
Exac | rs536588176 |
Gnomad | rs536588176 |
Varsome | rs536588176 |
LitVar | rs536588176 |
Map | rs536588176 |
PheGenI | rs536588176 |
Biobank | rs536588176 |
1000 genomes | rs536588176 |
hgdp | rs536588176 |
ensembl | rs536588176 |
geneview | rs536588176 |
scholar | rs536588176 |
rs536588176 | |
pharmgkb | rs536588176 |
gwascentral | rs536588176 |
openSNP | rs536588176 |
23andMe | rs536588176 |
SNPshot | rs536588176 |
SNPdbe | rs536588176 |
MSV3d | rs536588176 |
GWAS Ctlg | rs536588176 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs536588176(G;G) rs536588176(T;T) |
Alt | rs536588176(G;G) rs536588176(T;T) |
Reference | Rs536588176(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | FBN1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.48812912C>G |
CLNSRC | |
CLNACC | RCV000181425.1, |