rs532876832
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs532876832(A;A) |
| Make rs532876832(A;G) |
| Make rs532876832(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 21 |
| Position | 25881337 |
| Gene | APP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs532876832 |
| dbSNP (classic) | rs532876832 |
| ClinGen | rs532876832 |
| ebi | rs532876832 |
| HLI | rs532876832 |
| Exac | rs532876832 |
| Gnomad | rs532876832 |
| Varsome | rs532876832 |
| LitVar | rs532876832 |
| Map | rs532876832 |
| PheGenI | rs532876832 |
| Biobank | rs532876832 |
| 1000 genomes | rs532876832 |
| hgdp | rs532876832 |
| ensembl | rs532876832 |
| geneview | rs532876832 |
| scholar | rs532876832 |
| rs532876832 | |
| pharmgkb | rs532876832 |
| gwascentral | rs532876832 |
| openSNP | rs532876832 |
| 23andMe | rs532876832 |
| SNPshot | rs532876832 |
| SNPdbe | rs532876832 |
| MSV3d | rs532876832 |
| GWAS Ctlg | rs532876832 |
| Max Magnitude | 0 |
[PMID 27569544
] A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease. This SNP maps to a position listed in Table S6 as a non-coding variant that their biocurators felt was convincingly associated with a Mendelian disease.
