rs28931576
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs28931576(A;G) |
Make rs28931576(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 44907894 |
Gene | APOE |
is a | snp |
is | mentioned by |
dbSNP | rs28931576 |
dbSNP (classic) | rs28931576 |
ClinGen | rs28931576 |
ebi | rs28931576 |
HLI | rs28931576 |
Exac | rs28931576 |
Gnomad | rs28931576 |
Varsome | rs28931576 |
LitVar | rs28931576 |
Map | rs28931576 |
PheGenI | rs28931576 |
Biobank | rs28931576 |
1000 genomes | rs28931576 |
hgdp | rs28931576 |
ensembl | rs28931576 |
geneview | rs28931576 |
scholar | rs28931576 |
rs28931576 | |
pharmgkb | rs28931576 |
gwascentral | rs28931576 |
openSNP | rs28931576 |
23andMe | rs28931576 |
SNPshot | rs28931576 |
SNPdbe | rs28931576 |
MSV3d | rs28931576 |
GWAS Ctlg | rs28931576 |
Max Magnitude | 0 |
The ancestral allele is A.
ClinVar | |
---|---|
Risk | rs28931576(G;G) |
Alt | rs28931576(G;G) |
Reference | Rs28931576(A;A) |
Significance | Pathogenic |
Disease | APOE3(-)-FREIBURG |
Variation | info |
Gene | APOE |
CLNDBN | APOE3(-)-FREIBURG |
Reversed | 0 |
HGVS | NC_000019.9:g.45411151A>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000019457.23, |