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, |