rs1052352
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs1052352(C;T) |
| Make rs1052352(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 31183958 |
| Gene | FUS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1052352 |
| dbSNP (classic) | rs1052352 |
| ClinGen | rs1052352 |
| ebi | rs1052352 |
| HLI | rs1052352 |
| Exac | rs1052352 |
| Gnomad | rs1052352 |
| Varsome | rs1052352 |
| LitVar | rs1052352 |
| Map | rs1052352 |
| PheGenI | rs1052352 |
| Biobank | rs1052352 |
| 1000 genomes | rs1052352 |
| hgdp | rs1052352 |
| ensembl | rs1052352 |
| geneview | rs1052352 |
| scholar | rs1052352 |
| rs1052352 | |
| pharmgkb | rs1052352 |
| gwascentral | rs1052352 |
| openSNP | rs1052352 |
| 23andMe | rs1052352 |
| SNPshot | rs1052352 |
| SNPdbe | rs1052352 |
| MSV3d | rs1052352 |
| GWAS Ctlg | rs1052352 |
| GMAF | 0.4646 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20061612] FUS/TLS genetic variability in sporadic frontotemporal lobar degeneration
| ClinVar | |
|---|---|
| Risk | rs1052352(T;T) |
| Alt | rs1052352(T;T) |
| Reference | Rs1052352(C;C) |
| Significance | Non-pathogenic |
| Disease | not specified Amyotrophic Lateral Sclerosis |
| Variation | info |
| Gene | FUS |
| CLNDBN | not specified Amyotrophic Lateral Sclerosis, Dominant |
| Reversed | 0 |
| HGVS | NC_000016.9:g.31195279C>T |
| CLNSRC | |
| CLNACC | RCV000244413.1, RCV000277026.1, |
