rs140808909
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs140808909(A;A) |
Make rs140808909(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 44909080 |
Gene | APOE |
is a | snp |
is | mentioned by |
dbSNP | rs140808909 |
dbSNP (classic) | rs140808909 |
ClinGen | rs140808909 |
ebi | rs140808909 |
HLI | rs140808909 |
Exac | rs140808909 |
Gnomad | rs140808909 |
Varsome | rs140808909 |
LitVar | rs140808909 |
Map | rs140808909 |
PheGenI | rs140808909 |
Biobank | rs140808909 |
1000 genomes | rs140808909 |
hgdp | rs140808909 |
ensembl | rs140808909 |
geneview | rs140808909 |
scholar | rs140808909 |
rs140808909 | |
pharmgkb | rs140808909 |
gwascentral | rs140808909 |
openSNP | rs140808909 |
23andMe | rs140808909 |
SNPshot | rs140808909 |
SNPdbe | rs140808909 |
MSV3d | rs140808909 |
GWAS Ctlg | rs140808909 |
GMAF | 0.0009183 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs140808909(A;A) |
Alt | rs140808909(A;A) |
Reference | Rs140808909(G;G) |
Significance | Pathogenic |
Disease | Familial type 3 hyperlipoproteinemia |
Variation | info |
Gene | APOE |
CLNDBN | Familial type 3 hyperlipoproteinemia |
Reversed | 0 |
HGVS | NC_000019.9:g.45412337G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000019435.30, |