rs1056917
From SNPedia
| Orientation | minus |
| Make rs1056917(C;C) |
| Make rs1056917(C;T) |
| Make rs1056917(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 19 |
| Position | 49016209 |
| Gene | LHB, RUVBL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1056917 |
| dbSNP (classic) | rs1056917 |
| ClinGen | rs1056917 |
| ebi | rs1056917 |
| HLI | rs1056917 |
| Exac | rs1056917 |
| Gnomad | rs1056917 |
| Varsome | rs1056917 |
| LitVar | rs1056917 |
| Map | rs1056917 |
| PheGenI | rs1056917 |
| Biobank | rs1056917 |
| 1000 genomes | rs1056917 |
| hgdp | rs1056917 |
| ensembl | rs1056917 |
| geneview | rs1056917 |
| scholar | rs1056917 |
| rs1056917 | |
| pharmgkb | rs1056917 |
| gwascentral | rs1056917 |
| openSNP | rs1056917 |
| 23andMe | rs1056917 |
| SNPshot | rs1056917 |
| SNPdbe | rs1056917 |
| MSV3d | rs1056917 |
| GWAS Ctlg | rs1056917 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 30958034] Association of Luteinizing hormone and LH receptor gene polymorphism with susceptibility of Polycystic ovary syndrome.
