rs362771
From SNPedia
Orientation | plus |
Make rs362771(C;C) |
Make rs362771(C;T) |
Make rs362771(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 7 |
Position | 103548441 |
Gene | RELN |
is a | snp |
is | mentioned by |
dbSNP | rs362771 |
dbSNP (classic) | rs362771 |
ClinGen | rs362771 |
ebi | rs362771 |
HLI | rs362771 |
Exac | rs362771 |
Gnomad | rs362771 |
Varsome | rs362771 |
LitVar | rs362771 |
Map | rs362771 |
PheGenI | rs362771 |
Biobank | rs362771 |
1000 genomes | rs362771 |
hgdp | rs362771 |
ensembl | rs362771 |
geneview | rs362771 |
scholar | rs362771 |
rs362771 | |
pharmgkb | rs362771 |
gwascentral | rs362771 |
openSNP | rs362771 |
23andMe | rs362771 |
SNPshot | rs362771 |
SNPdbe | rs362771 |
MSV3d | rs362771 |
GWAS Ctlg | rs362771 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 30704480] Identification of exon skipping events associated with Alzheimer's disease in the human hippocampus.