rs886063161
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (ACTTCTACAAA;ACTTCTACAAA) | 0 | common in clinvar |
| Chromosome | 8 |
| Position | 86654019 |
| Gene | CNGB3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs886063161 |
| dbSNP (classic) | rs886063161 |
| ClinGen | rs886063161 |
| ebi | rs886063161 |
| HLI | rs886063161 |
| Exac | rs886063161 |
| Gnomad | rs886063161 |
| Varsome | rs886063161 |
| LitVar | rs886063161 |
| Map | rs886063161 |
| PheGenI | rs886063161 |
| Biobank | rs886063161 |
| 1000 genomes | rs886063161 |
| hgdp | rs886063161 |
| ensembl | rs886063161 |
| geneview | rs886063161 |
| scholar | rs886063161 |
| rs886063161 | |
| pharmgkb | rs886063161 |
| gwascentral | rs886063161 |
| openSNP | rs886063161 |
| 23andMe | rs886063161 |
| SNPshot | rs886063161 |
| SNPdbe | rs886063161 |
| MSV3d | rs886063161 |
| GWAS Ctlg | rs886063161 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs886063161(T;T) |
| Alt | rs886063161(T;T) |
| Reference | Rs886063161(ACTTCTACAAA;ACTTCTACAAA) |
| Significance | Probable-Pathogenic |
| Disease | CNGB3-Related Disorders |
| Variation | info |
| Gene | CNGB3 |
| CLNDBN | CNGB3-Related Disorders |
| Reversed | 1 |
| HGVS | NC_000008.10:g.87666247_87666257delTTTGTAGAAGTinsA |
| CLNSRC | Illumina |
| CLNACC | RCV000278041.1, |
