rs144564120
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (G;G) | 0 | common in clinvar | 
| Make rs144564120(C;C) | 
| Make rs144564120(C;G) | 
| Reference | GRCh38.p7 38.3/149 | 
| Chromosome | 19 | 
| Position | 45352249 | 
| Gene | ERCC2 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs144564120 | 
| dbSNP (classic) | rs144564120 | 
| ClinGen | rs144564120 | 
| ebi | rs144564120 | 
| HLI | rs144564120 | 
| Exac | rs144564120 | 
| Gnomad | rs144564120 | 
| Varsome | rs144564120 | 
| LitVar | rs144564120 | 
| Map | rs144564120 | 
| PheGenI | rs144564120 | 
| Biobank | rs144564120 | 
| 1000 genomes | rs144564120 | 
| hgdp | rs144564120 | 
| ensembl | rs144564120 | 
| geneview | rs144564120 | 
| scholar | rs144564120 | 
| rs144564120 | |
| pharmgkb | rs144564120 | 
| gwascentral | rs144564120 | 
| openSNP | rs144564120 | 
| 23andMe | rs144564120 | 
| SNPshot | rs144564120 | 
| SNPdbe | rs144564120 | 
| MSV3d | rs144564120 | 
| GWAS Ctlg | rs144564120 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs144564120(C;C) | 
| Alt | rs144564120(C;C) | 
| Reference | Rs144564120(G;G) | 
| Significance | Pathogenic | 
| Disease | not specified not provided | 
| Variation | info | 
| Gene | ERCC2 | 
| CLNDBN | not specified not provided | 
| Reversed | 0 | 
| HGVS | NC_000019.9:g.45855507G>C | 
| CLNSRC | |
| CLNACC | RCV000120774.1, RCV000255243.1, | 


