rs137852703
From SNPedia
Merged into | rs28936380 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;G) | ||
(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 226885546 |
Gene | PSEN2 |
is a | snp |
is | mentioned by |
dbSNP | rs137852703 |
dbSNP (classic) | rs137852703 |
ClinGen | rs137852703 |
ebi | rs137852703 |
HLI | rs137852703 |
Exac | rs137852703 |
Gnomad | rs137852703 |
Varsome | rs137852703 |
LitVar | rs137852703 |
Map | rs137852703 |
PheGenI | rs137852703 |
Biobank | rs137852703 |
1000 genomes | rs137852703 |
hgdp | rs137852703 |
ensembl | rs137852703 |
geneview | rs137852703 |
scholar | rs137852703 |
rs137852703 | |
pharmgkb | rs137852703 |
gwascentral | rs137852703 |
openSNP | rs137852703 |
23andMe | rs137852703 |
SNPshot | rs137852703 |
SNPdbe | rs137852703 |
MSV3d | rs137852703 |
GWAS Ctlg | rs137852703 |
Status | Merged into rs28936380 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | Rs137852703(G;G) |
Alt | Rs137852703(G;G) |
Reference | Rs137852703(C;C) |
Significance | Pathogenic |
Disease | Alzheimer disease |
Variation | info |
Gene | PSEN2 |
CLNDBN | Alzheimer disease, type 4 |
Reversed | 0 |
HGVS | NC_000001.10:g.227073247C>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | SCV000029617.1, |