rs704180
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs704180(A;A) |
Make rs704180(A;G) |
Make rs704180(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 21841177 |
Gene | ABCC9 |
is a | snp |
is | mentioned by |
dbSNP | rs704180 |
dbSNP (classic) | rs704180 |
ClinGen | rs704180 |
ebi | rs704180 |
HLI | rs704180 |
Exac | rs704180 |
Gnomad | rs704180 |
Varsome | rs704180 |
LitVar | rs704180 |
Map | rs704180 |
PheGenI | rs704180 |
Biobank | rs704180 |
1000 genomes | rs704180 |
hgdp | rs704180 |
ensembl | rs704180 |
geneview | rs704180 |
scholar | rs704180 |
rs704180 | |
pharmgkb | rs704180 |
gwascentral | rs704180 |
openSNP | rs704180 |
23andMe | rs704180 |
SNPshot | rs704180 |
SNPdbe | rs704180 |
MSV3d | rs704180 |
GWAS Ctlg | rs704180 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25470345] Reassessment of risk genotypes (GRN, TMEM106B, and ABCC9 variants) associated with hippocampal sclerosis of aging pathology
[PMID 26115089] Novel human ABCC9/SUR2 brain expressed transcripts and an eQTL relevant to hippocampal sclerosis of aging
[PMID 28189700] CSF protein changes associated with hippocampal sclerosis risk gene variants highlight impact of GRN/PGRN.