rs387906571
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs387906571(C;C) |
Make rs387906571(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 116836094 |
Gene | APOA1, APOA1-AS |
is a | snp |
is | mentioned by |
dbSNP | rs387906571 |
dbSNP (classic) | rs387906571 |
ClinGen | rs387906571 |
ebi | rs387906571 |
HLI | rs387906571 |
Exac | rs387906571 |
Gnomad | rs387906571 |
Varsome | rs387906571 |
LitVar | rs387906571 |
Map | rs387906571 |
PheGenI | rs387906571 |
Biobank | rs387906571 |
1000 genomes | rs387906571 |
hgdp | rs387906571 |
ensembl | rs387906571 |
geneview | rs387906571 |
scholar | rs387906571 |
rs387906571 | |
pharmgkb | rs387906571 |
gwascentral | rs387906571 |
openSNP | rs387906571 |
23andMe | rs387906571 |
SNPshot | rs387906571 |
SNPdbe | rs387906571 |
MSV3d | rs387906571 |
GWAS Ctlg | rs387906571 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906571(C;C) |
Alt | rs387906571(C;C) |
Reference | Rs387906571(G;G) |
Significance | Pathogenic |
Disease | Amyloidosis |
Variation | info |
Gene | APOA1-AS APOA1 |
CLNDBN | Amyloidosis, cardiac and cutaneous |
Reversed | 1 |
HGVS | NC_000011.9:g.116706810C>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000019525.28, |