Have questions? Visit https://www.reddit.com/r/SNPedia

rs144564120

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs144564120(C;C)
Make rs144564120(C;G)
ReferenceGRCh38.p7 38.3/149
Chromosome19
Position45352249
GeneERCC2
is asnp
is mentioned by
dbSNPrs144564120
dbSNP (classic)rs144564120
ClinGenrs144564120
ebirs144564120
HLIrs144564120
Exacrs144564120
Gnomadrs144564120
Varsomers144564120
LitVarrs144564120
Maprs144564120
PheGenIrs144564120
Biobankrs144564120
1000 genomesrs144564120
hgdprs144564120
ensemblrs144564120
geneviewrs144564120
scholarrs144564120
googlers144564120
pharmgkbrs144564120
gwascentralrs144564120
openSNPrs144564120
23andMers144564120
23andMe allrs144564120
SNPshotrs144564120
SNPdbers144564120
MSV3drs144564120
GWAS Ctlgrs144564120
Max Magnitude0
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,