rs756994701
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs756994701(A;A) |
| Make rs756994701(A;G) |
| Make rs756994701(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 9 |
| Position | 127854365 |
| Gene | ENG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs756994701 |
| dbSNP (classic) | rs756994701 |
| ClinGen | rs756994701 |
| ebi | rs756994701 |
| HLI | rs756994701 |
| Exac | rs756994701 |
| Gnomad | rs756994701 |
| Varsome | rs756994701 |
| LitVar | rs756994701 |
| Map | rs756994701 |
| PheGenI | rs756994701 |
| Biobank | rs756994701 |
| 1000 genomes | rs756994701 |
| hgdp | rs756994701 |
| ensembl | rs756994701 |
| geneview | rs756994701 |
| scholar | rs756994701 |
| rs756994701 | |
| pharmgkb | rs756994701 |
| gwascentral | rs756994701 |
| openSNP | rs756994701 |
| 23andMe | rs756994701 |
| SNPshot | rs756994701 |
| SNPdbe | rs756994701 |
| MSV3d | rs756994701 |
| GWAS Ctlg | rs756994701 |
| 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.
