rs1800447
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs1800447(C;C) |
| Make rs1800447(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 19 |
| Position | 49016648 |
| Gene | LHB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1800447 |
| dbSNP (classic) | rs1800447 |
| ClinGen | rs1800447 |
| ebi | rs1800447 |
| HLI | rs1800447 |
| Exac | rs1800447 |
| Gnomad | rs1800447 |
| Varsome | rs1800447 |
| LitVar | rs1800447 |
| Map | rs1800447 |
| PheGenI | rs1800447 |
| Biobank | rs1800447 |
| 1000 genomes | rs1800447 |
| hgdp | rs1800447 |
| ensembl | rs1800447 |
| geneview | rs1800447 |
| scholar | rs1800447 |
| rs1800447 | |
| pharmgkb | rs1800447 |
| gwascentral | rs1800447 |
| openSNP | rs1800447 |
| 23andMe | rs1800447 |
| SNPshot | rs1800447 |
| SNPdbe | rs1800447 |
| MSV3d | rs1800447 |
| GWAS Ctlg | rs1800447 |
| GMAF | 0.06152 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs1800447(C;C) |
| Alt | rs1800447(C;C) |
| Reference | Rs1800447(T;T) |
| Significance | Non-pathogenic |
| Disease | LUTEINIZING HORMONE POLYMORPHISM |
| Variation | info |
| Gene | LHB |
| CLNDBN | LUTEINIZING HORMONE POLYMORPHISM |
| Reversed | 1 |
| HGVS | NC_000019.9:g.49519905A>G |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000015495.3, |
[PMID 18439297
] A luteinizing hormone receptor intronic variant is significantly associated with decreased risk of Alzheimer's disease in males carrying an apolipoprotein E epsilon4 allele.
[PMID 18603647] Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.
