rs638944
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs638944(G;G) |
| Make rs638944(G;T) |
| Make rs638944(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 54876242 |
| Gene | DHCR24 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs638944 |
| dbSNP (classic) | rs638944 |
| ClinGen | rs638944 |
| ebi | rs638944 |
| HLI | rs638944 |
| Exac | rs638944 |
| Gnomad | rs638944 |
| Varsome | rs638944 |
| LitVar | rs638944 |
| Map | rs638944 |
| PheGenI | rs638944 |
| Biobank | rs638944 |
| 1000 genomes | rs638944 |
| hgdp | rs638944 |
| ensembl | rs638944 |
| geneview | rs638944 |
| scholar | rs638944 |
| rs638944 | |
| pharmgkb | rs638944 |
| gwascentral | rs638944 |
| openSNP | rs638944 |
| 23andMe | rs638944 |
| SNPshot | rs638944 |
| SNPdbe | rs638944 |
| MSV3d | rs638944 |
| GWAS Ctlg | rs638944 |
| GMAF | 0.4761 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 17510943] rs638944(T) and rs600491(C) Alzheimer's disease protective haplotype TC with frequency of 0.22 in cases and 0.30 in controls (P < 0.001)
[PMID 17510943] rs638944(G) and rs600491(C) Alzheimer's disease risk haplotype GC with frequency of 0.10 in cases and 0.05 in controls (P < 0.001)
[PMID 15986317
] Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.
