rs12628
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs12628(C;C) |
| Make rs12628(C;T) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 11 |
| Position | 534242 |
| Gene | HRAS, LRRC56 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12628 |
| dbSNP (classic) | rs12628 |
| ClinGen | rs12628 |
| ebi | rs12628 |
| HLI | rs12628 |
| Exac | rs12628 |
| Gnomad | rs12628 |
| Varsome | rs12628 |
| LitVar | rs12628 |
| Map | rs12628 |
| PheGenI | rs12628 |
| Biobank | rs12628 |
| 1000 genomes | rs12628 |
| hgdp | rs12628 |
| ensembl | rs12628 |
| geneview | rs12628 |
| scholar | rs12628 |
| rs12628 | |
| pharmgkb | rs12628 |
| gwascentral | rs12628 |
| openSNP | rs12628 |
| 23andMe | rs12628 |
| SNPshot | rs12628 |
| SNPdbe | rs12628 |
| MSV3d | rs12628 |
| GWAS Ctlg | rs12628 |
| GMAF | 0.2971 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22618666
] Association between HRAS rs12628 and rs112587690 polymorphisms with the risk of melanoma in the North American population
[PMID 16835863] Paternal bias in parental origin of HRAS mutations in Costello syndrome.
| ClinVar | |
|---|---|
| Risk | rs12628(C;C) |
| Alt | rs12628(C;C) |
| Reference | Rs12628(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified Rasopathy |
| Variation | info |
| Gene | HRAS |
| CLNDBN | not specified Rasopathy |
| Reversed | 1 |
| HGVS | NC_000011.9:g.534242A>G |
| CLNSRC | HGMD |
| CLNACC | RCV000038468.7, RCV000149841.1, |
[PMID 33390813] Association analysis between the interaction of RAS family genes mutations and papillary thyroid carcinoma in the Han Chinese population.
