rs35211634
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs35211634(C;C) |
| Make rs35211634(C;T) |
| Make rs35211634(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 59845386 |
| Gene | GIF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35211634 |
| dbSNP (classic) | rs35211634 |
| ClinGen | rs35211634 |
| ebi | rs35211634 |
| HLI | rs35211634 |
| Exac | rs35211634 |
| Gnomad | rs35211634 |
| Varsome | rs35211634 |
| LitVar | rs35211634 |
| Map | rs35211634 |
| PheGenI | rs35211634 |
| Biobank | rs35211634 |
| 1000 genomes | rs35211634 |
| hgdp | rs35211634 |
| ensembl | rs35211634 |
| geneview | rs35211634 |
| scholar | rs35211634 |
| rs35211634 | |
| pharmgkb | rs35211634 |
| gwascentral | rs35211634 |
| openSNP | rs35211634 |
| 23andMe | rs35211634 |
| SNPshot | rs35211634 |
| SNPdbe | rs35211634 |
| MSV3d | rs35211634 |
| GWAS Ctlg | rs35211634 |
| GMAF | 0.08494 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs35211634(C;C) |
| Alt | rs35211634(C;C) |
| Reference | rs35211634(T;T) |
| Significance | Other |
| Disease | Intrinsic factor deficiency Intrinsic factor deficiency |
| Variation | info |
| Gene | GIF |
| CLNDBN | Intrinsic factor deficiency, congenital, susceptibility to Intrinsic factor deficiency |
| Reversed | 0 |
| HGVS | NC_000011.9:g.59612859T>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000001812.2, RCV000346011.1, |
