rs267599193
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (C;C) | 0 | common in clinvar | 
| Make rs267599193(C;T) | 
| Make rs267599193(T;T) | 
| Reference | GRCh38.p7 38.3/150 | 
| Chromosome | 2 | 
| Position | 211713583 | 
| Gene | ERBB4 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs267599193 | 
| dbSNP (classic) | rs267599193 | 
| ClinGen | rs267599193 | 
| ebi | rs267599193 | 
| HLI | rs267599193 | 
| Exac | rs267599193 | 
| Gnomad | rs267599193 | 
| Varsome | rs267599193 | 
| LitVar | rs267599193 | 
| Map | rs267599193 | 
| PheGenI | rs267599193 | 
| Biobank | rs267599193 | 
| 1000 genomes | rs267599193 | 
| hgdp | rs267599193 | 
| ensembl | rs267599193 | 
| geneview | rs267599193 | 
| scholar | rs267599193 | 
| rs267599193 | |
| pharmgkb | rs267599193 | 
| gwascentral | rs267599193 | 
| openSNP | rs267599193 | 
| 23andMe | rs267599193 | 
| SNPshot | rs267599193 | 
| SNPdbe | rs267599193 | 
| MSV3d | rs267599193 | 
| GWAS Ctlg | rs267599193 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs267599193(T;T) | 
| Alt | rs267599193(T;T) | 
| Reference | Rs267599193(C;C) | 
| Significance | Probable-Pathogenic | 
| Disease | Malignant melanoma | 
| Variation | info | 
| Gene | ERBB4 | 
| CLNDBN | Malignant melanoma | 
| Reversed | 0 | 
| HGVS | NC_000002.11:g.212578308C>T | 
| CLNSRC | |
| CLNACC | RCV000435571.1, | 


