rs769065721
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs769065721(C;C) |
| Make rs769065721(C;G) |
| Make rs769065721(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 90916786 |
| Gene | ZNF644 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769065721 |
| dbSNP (classic) | rs769065721 |
| ClinGen | rs769065721 |
| ebi | rs769065721 |
| HLI | rs769065721 |
| Exac | rs769065721 |
| Gnomad | rs769065721 |
| Varsome | rs769065721 |
| LitVar | rs769065721 |
| Map | rs769065721 |
| PheGenI | rs769065721 |
| Biobank | rs769065721 |
| 1000 genomes | rs769065721 |
| hgdp | rs769065721 |
| ensembl | rs769065721 |
| geneview | rs769065721 |
| scholar | rs769065721 |
| rs769065721 | |
| pharmgkb | rs769065721 |
| gwascentral | rs769065721 |
| openSNP | rs769065721 |
| 23andMe | rs769065721 |
| SNPshot | rs769065721 |
| SNPdbe | rs769065721 |
| MSV3d | rs769065721 |
| GWAS Ctlg | rs769065721 |
| Max Magnitude | 0 |
[PMID 27569544
] A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease. This SNP maps to a position listed in Table S6 as a non-coding variant that their biocurators felt was convincingly associated with a Mendelian disease.
