rs6923492
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs6923492(C;C) |
| Make rs6923492(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 146434188 |
| Gene | GRM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6923492 |
| dbSNP (classic) | rs6923492 |
| ClinGen | rs6923492 |
| ebi | rs6923492 |
| HLI | rs6923492 |
| Exac | rs6923492 |
| Gnomad | rs6923492 |
| Varsome | rs6923492 |
| LitVar | rs6923492 |
| Map | rs6923492 |
| PheGenI | rs6923492 |
| Biobank | rs6923492 |
| 1000 genomes | rs6923492 |
| hgdp | rs6923492 |
| ensembl | rs6923492 |
| geneview | rs6923492 |
| scholar | rs6923492 |
| rs6923492 | |
| pharmgkb | rs6923492 |
| gwascentral | rs6923492 |
| openSNP | rs6923492 |
| 23andMe | rs6923492 |
| SNPshot | rs6923492 |
| SNPdbe | rs6923492 |
| MSV3d | rs6923492 |
| GWAS Ctlg | rs6923492 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24442360] Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders
| ClinVar | |
|---|---|
| Risk | rs6923492(C;C) |
| Alt | rs6923492(C;C) |
| Reference | Rs6923492(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | GRM1 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000006.11:g.146755324T>C |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000117205.2, |
