rs754594235
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs754594235(A;A) |
| Make rs754594235(A;C) |
| Make rs754594235(C;C) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 80169007 |
| Gene | ANXA11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs754594235 |
| dbSNP (classic) | rs754594235 |
| ClinGen | rs754594235 |
| ebi | rs754594235 |
| HLI | rs754594235 |
| Exac | rs754594235 |
| Gnomad | rs754594235 |
| Varsome | rs754594235 |
| LitVar | rs754594235 |
| Map | rs754594235 |
| PheGenI | rs754594235 |
| Biobank | rs754594235 |
| 1000 genomes | rs754594235 |
| hgdp | rs754594235 |
| ensembl | rs754594235 |
| geneview | rs754594235 |
| scholar | rs754594235 |
| rs754594235 | |
| pharmgkb | rs754594235 |
| gwascentral | rs754594235 |
| openSNP | rs754594235 |
| 23andMe | rs754594235 |
| SNPshot | rs754594235 |
| SNPdbe | rs754594235 |
| MSV3d | rs754594235 |
| GWAS Ctlg | rs754594235 |
| Max Magnitude | 0 |
aka NM_145869.1(ANXA11):c.523G>A or (p.Gly175Arg)
OMIM pathogenic variant
