rs1114167892
From SNPedia
| Orientation | minus |
| Make rs1114167892(C;C) |
| Make rs1114167892(C;T) |
| Make rs1114167892(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 21 |
| Position | 44330298 |
| Gene | CFAP410 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1114167892 |
| dbSNP (classic) | rs1114167892 |
| ClinGen | rs1114167892 |
| ebi | rs1114167892 |
| HLI | rs1114167892 |
| Exac | rs1114167892 |
| Gnomad | rs1114167892 |
| Varsome | rs1114167892 |
| LitVar | rs1114167892 |
| Map | rs1114167892 |
| PheGenI | rs1114167892 |
| Biobank | rs1114167892 |
| 1000 genomes | rs1114167892 |
| hgdp | rs1114167892 |
| ensembl | rs1114167892 |
| geneview | rs1114167892 |
| scholar | rs1114167892 |
| rs1114167892 | |
| pharmgkb | rs1114167892 |
| gwascentral | rs1114167892 |
| openSNP | rs1114167892 |
| 23andMe | rs1114167892 |
| SNPshot | rs1114167892 |
| SNPdbe | rs1114167892 |
| MSV3d | rs1114167892 |
| GWAS Ctlg | rs1114167892 |
| Max Magnitude | 0 |
OMIM pathogenic
