rs71645922
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs71645922(A;A) |
| Make rs71645922(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 45476581 |
| Gene | LARS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs71645922 |
| dbSNP (classic) | rs71645922 |
| ClinGen | rs71645922 |
| ebi | rs71645922 |
| HLI | rs71645922 |
| Exac | rs71645922 |
| Gnomad | rs71645922 |
| Varsome | rs71645922 |
| LitVar | rs71645922 |
| Map | rs71645922 |
| PheGenI | rs71645922 |
| Biobank | rs71645922 |
| 1000 genomes | rs71645922 |
| hgdp | rs71645922 |
| ensembl | rs71645922 |
| geneview | rs71645922 |
| scholar | rs71645922 |
| rs71645922 | |
| pharmgkb | rs71645922 |
| gwascentral | rs71645922 |
| openSNP | rs71645922 |
| 23andMe | rs71645922 |
| SNPshot | rs71645922 |
| SNPdbe | rs71645922 |
| MSV3d | rs71645922 |
| GWAS Ctlg | rs71645922 |
| GMAF | 0.01561 |
| Max Magnitude | 0 |
A 2009 study of 11,163 Dutch participants found no evidence to support previous data indicating a role for SNPs in this gene (LARS2) in type 2 diabetes susceptibility.[PMID 19847392
]
| ClinVar | |
|---|---|
| Risk | rs71645922(A;A) |
| Alt | rs71645922(A;A) |
| Reference | Rs71645922(C;C) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | LARS2 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000003.11:g.45518073C>A |
| CLNSRC | |
| CLNACC | RCV000220287.2, |
