rs587777762
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587777762(-;-) |
Make rs587777762(-;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 154585800 |
Gene | FGA |
is a | snp |
is | mentioned by |
dbSNP | rs587777762 |
dbSNP (classic) | rs587777762 |
ClinGen | rs587777762 |
ebi | rs587777762 |
HLI | rs587777762 |
Exac | rs587777762 |
Gnomad | rs587777762 |
Varsome | rs587777762 |
LitVar | rs587777762 |
Map | rs587777762 |
PheGenI | rs587777762 |
Biobank | rs587777762 |
1000 genomes | rs587777762 |
hgdp | rs587777762 |
ensembl | rs587777762 |
geneview | rs587777762 |
scholar | rs587777762 |
rs587777762 | |
pharmgkb | rs587777762 |
gwascentral | rs587777762 |
openSNP | rs587777762 |
23andMe | rs587777762 |
SNPshot | rs587777762 |
SNPdbe | rs587777762 |
MSV3d | rs587777762 |
GWAS Ctlg | rs587777762 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777762(-;-) |
Alt | rs587777762(-;-) |
Reference | Rs587777762(C;C) |
Significance | Pathogenic |
Disease | Familial visceral amyloidosis |
Variation | info |
Gene | FGA |
CLNDBN | Familial visceral amyloidosis, Ostertag type |
Reversed | 0 |
HGVS | NC_000004.11:g.155506952delC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000017875.24, |