rs876661206
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs876661206(A;T) |
| Make rs876661206(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 2 |
| Position | 166204222 |
| Gene | LOC101929680, SCN9A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs876661206 |
| dbSNP (classic) | rs876661206 |
| ClinGen | rs876661206 |
| ebi | rs876661206 |
| HLI | rs876661206 |
| Exac | rs876661206 |
| Gnomad | rs876661206 |
| Varsome | rs876661206 |
| LitVar | rs876661206 |
| Map | rs876661206 |
| PheGenI | rs876661206 |
| Biobank | rs876661206 |
| 1000 genomes | rs876661206 |
| hgdp | rs876661206 |
| ensembl | rs876661206 |
| geneview | rs876661206 |
| scholar | rs876661206 |
| rs876661206 | |
| pharmgkb | rs876661206 |
| gwascentral | rs876661206 |
| openSNP | rs876661206 |
| 23andMe | rs876661206 |
| SNPshot | rs876661206 |
| SNPdbe | rs876661206 |
| MSV3d | rs876661206 |
| GWAS Ctlg | rs876661206 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs876661206(T;T) |
| Alt | rs876661206(T;T) |
| Reference | Rs876661206(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | LOC101929680 SCN9A |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000002.11:g.167060732T>A |
| CLNSRC | |
| CLNACC | RCV000220058.1, |
