rs63751392
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (I;I) | 0 | common genotype |
| Make rs63751392(-;-) |
| Make rs63751392(-;AAT) |
| Make rs63751392(AAT;AAT) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 17 |
| Position | 46010374 |
| Gene | MAPT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs63751392 |
| dbSNP (classic) | rs63751392 |
| ClinGen | rs63751392 |
| ebi | rs63751392 |
| HLI | rs63751392 |
| Exac | rs63751392 |
| Gnomad | rs63751392 |
| Varsome | rs63751392 |
| LitVar | rs63751392 |
| Map | rs63751392 |
| PheGenI | rs63751392 |
| Biobank | rs63751392 |
| 1000 genomes | rs63751392 |
| hgdp | rs63751392 |
| ensembl | rs63751392 |
| geneview | rs63751392 |
| scholar | rs63751392 |
| rs63751392 | |
| pharmgkb | rs63751392 |
| gwascentral | rs63751392 |
| openSNP | rs63751392 |
| 23andMe | rs63751392 |
| SNPshot | rs63751392 |
| SNPdbe | rs63751392 |
| MSV3d | rs63751392 |
| GWAS Ctlg | rs63751392 |
| Merged from | Rs199422218 |
| Max Magnitude | 0 |
aka NM_016835.4(MAPT):c.1838_1840delATA or (p.Asn613del)
OMIM pathogenic variant
