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rs376556895

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376556895(C;G)
Make rs376556895(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome19
Position45352801
GeneERCC2
is asnp
is mentioned by
dbSNPrs376556895
dbSNP (classic)rs376556895
ClinGenrs376556895
ebirs376556895
HLIrs376556895
Exacrs376556895
Gnomadrs376556895
Varsomers376556895
LitVarrs376556895
Maprs376556895
PheGenIrs376556895
Biobankrs376556895
1000 genomesrs376556895
hgdprs376556895
ensemblrs376556895
geneviewrs376556895
scholarrs376556895
googlers376556895
pharmgkbrs376556895
gwascentralrs376556895
openSNPrs376556895
23andMers376556895
SNPshotrs376556895
SNPdbers376556895
MSV3drs376556895
GWAS Ctlgrs376556895
Max Magnitude0
ClinVar
Risk rs376556895(G;G) rs376556895(T;T)
Alt rs376556895(G;G) rs376556895(T;T)
Reference Rs376556895(C;C)
Significance Pathogenic
Disease Xeroderma pigmentosum not provided
Variation info
Gene ERCC2
CLNDBN Xeroderma pigmentosum not provided
Reversed 0
HGVS NC_000019.9:g.45856059C>G
CLNSRC Illumina
CLNACC RCV000312948.1, RCV000489442.1,