rs200686732
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs200686732(C;T) |
| Make rs200686732(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 2 |
| Position | 43995941 |
| Gene | LRPPRC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs200686732 |
| dbSNP (classic) | rs200686732 |
| ClinGen | rs200686732 |
| ebi | rs200686732 |
| HLI | rs200686732 |
| Exac | rs200686732 |
| Gnomad | rs200686732 |
| Varsome | rs200686732 |
| LitVar | rs200686732 |
| Map | rs200686732 |
| PheGenI | rs200686732 |
| Biobank | rs200686732 |
| 1000 genomes | rs200686732 |
| hgdp | rs200686732 |
| ensembl | rs200686732 |
| geneview | rs200686732 |
| scholar | rs200686732 |
| rs200686732 | |
| pharmgkb | rs200686732 |
| gwascentral | rs200686732 |
| openSNP | rs200686732 |
| 23andMe | rs200686732 |
| SNPshot | rs200686732 |
| SNPdbe | rs200686732 |
| MSV3d | rs200686732 |
| GWAS Ctlg | rs200686732 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs200686732(A;A) rs200686732(G;G) rs200686732(T;T) |
| Alt | rs200686732(A;A) rs200686732(G;G) rs200686732(T;T) |
| Reference | Rs200686732(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | LRPPRC |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.44223080C>T |
| CLNSRC | |
| CLNACC | RCV000199897.1, |
