rs121907984
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs121907984(A;A) |
| Make rs121907984(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 74721131 |
| Gene | GFM2, HEXB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121907984 |
| dbSNP (classic) | rs121907984 |
| ClinGen | rs121907984 |
| ebi | rs121907984 |
| HLI | rs121907984 |
| Exac | rs121907984 |
| Gnomad | rs121907984 |
| Varsome | rs121907984 |
| LitVar | rs121907984 |
| Map | rs121907984 |
| PheGenI | rs121907984 |
| Biobank | rs121907984 |
| 1000 genomes | rs121907984 |
| hgdp | rs121907984 |
| ensembl | rs121907984 |
| geneview | rs121907984 |
| scholar | rs121907984 |
| rs121907984 | |
| pharmgkb | rs121907984 |
| gwascentral | rs121907984 |
| openSNP | rs121907984 |
| 23andMe | rs121907984 |
| SNPshot | rs121907984 |
| SNPdbe | rs121907984 |
| MSV3d | rs121907984 |
| GWAS Ctlg | rs121907984 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121907984(A;A) |
| Alt | rs121907984(A;A) |
| Reference | Rs121907984(G;G) |
| Significance | Other |
| Disease | HEXOSAMINIDASE B not provided |
| Variation | info |
| Gene | HEXB GFM2 |
| CLNDBN | HEXOSAMINIDASE B, HEAT-LABILE POLYMORPHISM not provided |
| Reversed | 0 |
| HGVS | NC_000005.9:g.74016956G>A |
| CLNSRC | HGMD OMIM Allelic Variant |
| CLNACC | RCV000004085.2, RCV000079061.5, |
