rs2279017

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs2279017(G;G)

Make rs2279017(G;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

14148737

Gene	LOC107986063, XPC

is a	snp
is	mentioned by
dbSNP	rs2279017
dbSNP (classic)	rs2279017
ClinGen	rs2279017
ebi	rs2279017
HLI	rs2279017
Exac	rs2279017
Gnomad	rs2279017
Varsome	rs2279017
LitVar	rs2279017
Map	rs2279017
PheGenI	rs2279017
Biobank	rs2279017
1000 genomes	rs2279017
hgdp	rs2279017
ensembl	rs2279017
geneview	rs2279017
scholar	rs2279017
google	rs2279017
pharmgkb	rs2279017
gwascentral	rs2279017
openSNP	rs2279017
23andMe	rs2279017
SNPshot	rs2279017
SNPdbe	rs2279017
MSV3d	rs2279017
GWAS Ctlg	rs2279017

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

[PMID 24939416] 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 Xeroderma pigmentosum
Variation	info
Gene	XPC
CLNDBN	not specified Xeroderma pigmentosum
Reversed	0
HGVS	NC_000003.11:g.14190237T>G
CLNSRC
CLNACC	RCV000170435.2, RCV000301008.1,