rs906807
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs906807(A;G) |
| Make rs906807(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 9117869 |
| Gene | NDUFV2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs906807 |
| dbSNP (classic) | rs906807 |
| ClinGen | rs906807 |
| ebi | rs906807 |
| HLI | rs906807 |
| Exac | rs906807 |
| Gnomad | rs906807 |
| Varsome | rs906807 |
| LitVar | rs906807 |
| Map | rs906807 |
| PheGenI | rs906807 |
| Biobank | rs906807 |
| 1000 genomes | rs906807 |
| hgdp | rs906807 |
| ensembl | rs906807 |
| geneview | rs906807 |
| scholar | rs906807 |
| rs906807 | |
| pharmgkb | rs906807 |
| gwascentral | rs906807 |
| openSNP | rs906807 |
| 23andMe | rs906807 |
| SNPshot | rs906807 |
| SNPdbe | rs906807 |
| MSV3d | rs906807 |
| GWAS Ctlg | rs906807 |
| GMAF | 0.2406 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19194776] Association study on the mitochondrial gene NDUFV2 and bipolar disorder in the Chinese Han population
| ClinVar | |
|---|---|
| Risk | rs906807(G;G) |
| Alt | rs906807(G;G) |
| Reference | Rs906807(A;A) |
| Significance | Other |
| Disease | Parkinson disease not specified Mitochondrial complex I deficiency |
| Variation | info |
| Gene | NDUFV2 |
| CLNDBN | Parkinson disease, mitochondrial not specified Mitochondrial complex I deficiency |
| Reversed | 1 |
| HGVS | NC_000018.9:g.9117867T>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000009621.2, RCV000117718.3, RCV000312272.1, |
[PMID 16436204
] GPNN: power studies and applications of a neural network method for detecting gene-gene interactions in studies of human disease.
[PMID 17601350] A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.
