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rs2470353

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2470353(C;C)
Make rs2470353(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position14148768
GeneLOC107986063, XPC
is asnp
is mentioned by
dbSNPrs2470353
dbSNP (old)rs2470353
ClinGenrs2470353
ebirs2470353
HLIrs2470353
Exacrs2470353
Gnomadrs2470353
Varsomers2470353
Maprs2470353
PheGenIrs2470353
Biobankrs2470353
1000 genomesrs2470353
hgdprs2470353
ensemblrs2470353
gopubmedrs2470353
geneviewrs2470353
scholarrs2470353
googlers2470353
pharmgkbrs2470353
gwascentralrs2470353
openSNPrs2470353
23andMers2470353
23andMe allrs2470353
SNP Nexus

SNPshotrs2470353
SNPdbers2470353
MSV3drs2470353
GWAS Ctlgrs2470353
GMAF0.3324
Max Magnitude0
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs2470353(A;A) rs2470353(C;C) rs2470353(T;T)
Alt rs2470353(A;A) rs2470353(C;C) rs2470353(T;T)
Reference Rs2470353(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene XPC
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.14190268G>C
CLNSRC
CLNACC RCV000248907.1,


[PMID 21273643OA-icon.png] In vitro functional effects of XPC gene rare variants from bladder cancer patients.