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rs773359656

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773359656(A;A)
Make rs773359656(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position45352646
GeneERCC2
is asnp
is mentioned by
dbSNPrs773359656
dbSNP (classic)rs773359656
ClinGenrs773359656
ebirs773359656
HLIrs773359656
Exacrs773359656
Gnomadrs773359656
Varsomers773359656
LitVarrs773359656
Maprs773359656
PheGenIrs773359656
Biobankrs773359656
1000 genomesrs773359656
hgdprs773359656
ensemblrs773359656
geneviewrs773359656
scholarrs773359656
googlers773359656
pharmgkbrs773359656
gwascentralrs773359656
openSNPrs773359656
23andMers773359656
23andMe allrs773359656
SNPshotrs773359656
SNPdbers773359656
MSV3drs773359656
GWAS Ctlgrs773359656
Max Magnitude0
ClinVar
Risk rs773359656(A;A)
Alt rs773359656(A;A)
Reference Rs773359656(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ERCC2
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.45855904G>A
CLNSRC
CLNACC RCV000494513.1,