rs148188503
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs148188503(C;T) |
| Make rs148188503(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 7 |
| Position | 55181364 |
| Gene | EGFR, EGFR-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs148188503 |
| dbSNP (classic) | rs148188503 |
| ClinGen | rs148188503 |
| ebi | rs148188503 |
| HLI | rs148188503 |
| Exac | rs148188503 |
| Gnomad | rs148188503 |
| Varsome | rs148188503 |
| LitVar | rs148188503 |
| Map | rs148188503 |
| PheGenI | rs148188503 |
| Biobank | rs148188503 |
| 1000 genomes | rs148188503 |
| hgdp | rs148188503 |
| ensembl | rs148188503 |
| geneview | rs148188503 |
| scholar | rs148188503 |
| rs148188503 | |
| pharmgkb | rs148188503 |
| gwascentral | rs148188503 |
| openSNP | rs148188503 |
| 23andMe | rs148188503 |
| SNPshot | rs148188503 |
| SNPdbe | rs148188503 |
| MSV3d | rs148188503 |
| GWAS Ctlg | rs148188503 |
| Max Magnitude | 0 |
[PMID 27895798
] Exploring the impact of EGFR T790M neighboring SNPs on ARMS-based T790M mutation assay.
| ClinVar | |
|---|---|
| Risk | rs148188503(T;T) |
| Alt | rs148188503(T;T) |
| Reference | Rs148188503(C;C) |
| Significance | Probable-non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | EGFR EGFR-AS1 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000007.13:g.55249057C>T |
| CLNSRC | |
| CLNACC | RCV000038426.2, |
