rs312262709
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs312262709(A;A) |
| Make rs312262709(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 44660607 |
| Gene | SPG11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs312262709 |
| dbSNP (classic) | rs312262709 |
| ClinGen | rs312262709 |
| ebi | rs312262709 |
| HLI | rs312262709 |
| Exac | rs312262709 |
| Gnomad | rs312262709 |
| Varsome | rs312262709 |
| LitVar | rs312262709 |
| Map | rs312262709 |
| PheGenI | rs312262709 |
| Biobank | rs312262709 |
| 1000 genomes | rs312262709 |
| hgdp | rs312262709 |
| ensembl | rs312262709 |
| geneview | rs312262709 |
| scholar | rs312262709 |
| rs312262709 | |
| pharmgkb | rs312262709 |
| gwascentral | rs312262709 |
| openSNP | rs312262709 |
| 23andMe | rs312262709 |
| SNPshot | rs312262709 |
| SNPdbe | rs312262709 |
| MSV3d | rs312262709 |
| GWAS Ctlg | rs312262709 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs312262709(A;A) |
| Alt | rs312262709(A;A) |
| Reference | Rs312262709(G;G) |
| Significance | Pathogenic |
| Disease | Spastic paraplegia 11 Amyotrophic lateral sclerosis type 5 |
| Variation | info |
| Gene | SPG11 |
| CLNDBN | Spastic paraplegia 11, autosomal recessive Amyotrophic lateral sclerosis type 5 |
| Reversed | 1 |
| HGVS | NC_000015.9:g.44952805C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000034195.2, RCV000194703.2, |
[PMID 18067136] Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia.
[PMID 18717728
] Clinical heterogeneity and genotype-phenotype correlations in hereditary spastic paraplegia because of Spatacsin mutations (SPG11).
