rs63750635
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs63750635(C;T) |
| Make rs63750635(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 46014286 |
| Gene | MAPT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs63750635 |
| dbSNP (classic) | rs63750635 |
| ClinGen | rs63750635 |
| ebi | rs63750635 |
| HLI | rs63750635 |
| Exac | rs63750635 |
| Gnomad | rs63750635 |
| Varsome | rs63750635 |
| LitVar | rs63750635 |
| Map | rs63750635 |
| PheGenI | rs63750635 |
| Biobank | rs63750635 |
| 1000 genomes | rs63750635 |
| hgdp | rs63750635 |
| ensembl | rs63750635 |
| geneview | rs63750635 |
| scholar | rs63750635 |
| rs63750635 | |
| pharmgkb | rs63750635 |
| gwascentral | rs63750635 |
| openSNP | rs63750635 |
| 23andMe | rs63750635 |
| SNPshot | rs63750635 |
| SNPdbe | rs63750635 |
| MSV3d | rs63750635 |
| GWAS Ctlg | rs63750635 |
| Max Magnitude | 0 |
| OMIM | 157140 |
| Desc | Pick's disease |
| Variant | 0018 |
| Related | also |
| ClinVar | |
|---|---|
| Risk | rs63750635(T;T) |
| Alt | rs63750635(T;T) |
| Reference | Rs63750635(C;C) |
| Significance | Pathogenic |
| Disease | Pick's disease not provided |
| Variation | info |
| Gene | MAPT |
| CLNDBN | Pick's disease not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.44091652C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000015331.26, RCV000084544.1, |
