rs12982192
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs12982192(C;C) |
Make rs12982192(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 44908002 |
Gene | APOE |
is a | snp |
is | mentioned by |
dbSNP | rs12982192 |
dbSNP (classic) | rs12982192 |
ClinGen | rs12982192 |
ebi | rs12982192 |
HLI | rs12982192 |
Exac | rs12982192 |
Gnomad | rs12982192 |
Varsome | rs12982192 |
LitVar | rs12982192 |
Map | rs12982192 |
PheGenI | rs12982192 |
Biobank | rs12982192 |
1000 genomes | rs12982192 |
hgdp | rs12982192 |
ensembl | rs12982192 |
geneview | rs12982192 |
scholar | rs12982192 |
rs12982192 | |
pharmgkb | rs12982192 |
gwascentral | rs12982192 |
openSNP | rs12982192 |
23andMe | rs12982192 |
SNPshot | rs12982192 |
SNPdbe | rs12982192 |
MSV3d | rs12982192 |
GWAS Ctlg | rs12982192 |
Max Magnitude | 0 |
[PMID 20822524] Isoform of APOE with retained intron 3; quantitation and identification of an associated single nucleotide polymorphism