rs74737358

Orientation

plus

Stabilized

plus

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

Make rs74737358(A;A)

Make rs74737358(A;C)

Make rs74737358(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

14158882

Gene

XPC

is a	snp
is	mentioned by
dbSNP	rs74737358
dbSNP (classic)	rs74737358
ClinGen	rs74737358
ebi	rs74737358
HLI	rs74737358
Exac	rs74737358
Gnomad	rs74737358
Varsome	rs74737358
LitVar	rs74737358
Map	rs74737358
PheGenI	rs74737358
Biobank	rs74737358
1000 genomes	rs74737358
hgdp	rs74737358
ensembl	rs74737358
geneview	rs74737358
scholar	rs74737358
google	rs74737358
pharmgkb	rs74737358
gwascentral	rs74737358
openSNP	rs74737358
23andMe	rs74737358
SNPshot	rs74737358
SNPdbe	rs74737358
MSV3d	rs74737358
GWAS Ctlg	rs74737358

GMAF

0.003673

Max Magnitude

0

OMIM	613208
Desc
Variant	0001
Related	also

ClinVar
Risk	rs74737358(A;A) rs74737358(C;C) rs74737358(T;T)
Alt	rs74737358(A;A) rs74737358(C;C) rs74737358(T;T)
Reference	Rs74737358(G;G)
Significance	Pathogenic
Disease	Xeroderma pigmentosum not specified
Variation	info
Gene	XPC
CLNDBN	Xeroderma pigmentosum, group C not specified
Reversed	0
HGVS	NC_000003.11:g.14200382G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000000277.2, RCV000122346.1,