rs2634073
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2634073(A;A) |
Make rs2634073(A;G) |
Make rs2634073(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 110744627 |
is a | snp |
is | mentioned by |
dbSNP | rs2634073 |
dbSNP (classic) | rs2634073 |
ClinGen | rs2634073 |
ebi | rs2634073 |
HLI | rs2634073 |
Exac | rs2634073 |
Gnomad | rs2634073 |
Varsome | rs2634073 |
LitVar | rs2634073 |
Map | rs2634073 |
PheGenI | rs2634073 |
Biobank | rs2634073 |
1000 genomes | rs2634073 |
hgdp | rs2634073 |
ensembl | rs2634073 |
geneview | rs2634073 |
scholar | rs2634073 |
rs2634073 | |
pharmgkb | rs2634073 |
gwascentral | rs2634073 |
openSNP | rs2634073 |
23andMe | rs2634073 |
SNPshot | rs2634073 |
SNPdbe | rs2634073 |
MSV3d | rs2634073 |
GWAS Ctlg | rs2634073 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25494715] Incidence of Dementia in Relation to Genetic Variants at PITX2, ZFHX3, and ApoE ε4 in Atrial Fibrillation Patients