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rs2279017

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2279017(G;G)
Make rs2279017(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position14148737
GeneXPC
is asnp
is mentioned by
dbSNPrs2279017
ebirs2279017
HLIrs2279017
Exacrs2279017
Varsomers2279017
Maprs2279017
PheGenIrs2279017
hapmaprs2279017
1000 genomesrs2279017
hgdprs2279017
ensemblrs2279017
gopubmedrs2279017
geneviewrs2279017
scholarrs2279017
googlers2279017
pharmgkbrs2279017
gwascentralrs2279017
openSNPrs2279017
23andMers2279017
23andMe allrs2279017
SNP Nexus

SNPshotrs2279017
SNPdbers2279017
MSV3drs2279017
GWAS Ctlgrs2279017
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 24939416OA-icon.png] CYP1A1 Ile462Val polymorphism and colorectal cancer risk in Polish patients


ClinVar
Risk rs2279017(G;G)
Alt rs2279017(G;G)
Reference rs2279017(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene XPC
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.14190237T>G
CLNSRC
CLNACC RCV000170435.1,