rs376556895

Orientation

plus

Stabilized

plus

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

Make rs376556895(C;G)

Make rs376556895(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

19

Position

45352801

Gene

ERCC2

is a	snp
is	mentioned by
dbSNP	rs376556895
dbSNP (classic)	rs376556895
ClinGen	rs376556895
ebi	rs376556895
HLI	rs376556895
Exac	rs376556895
Gnomad	rs376556895
Varsome	rs376556895
LitVar	rs376556895
Map	rs376556895
PheGenI	rs376556895
Biobank	rs376556895
1000 genomes	rs376556895
hgdp	rs376556895
ensembl	rs376556895
geneview	rs376556895
scholar	rs376556895
google	rs376556895
pharmgkb	rs376556895
gwascentral	rs376556895
openSNP	rs376556895
23andMe	rs376556895
SNPshot	rs376556895
SNPdbe	rs376556895
MSV3d	rs376556895
GWAS Ctlg	rs376556895

Max Magnitude

0

ClinVar
Risk	rs376556895(G;G) rs376556895(T;T)
Alt	rs376556895(G;G) rs376556895(T;T)
Reference	Rs376556895(C;C)
Significance	Pathogenic
Disease	Xeroderma pigmentosum not provided
Variation	info
Gene	ERCC2
CLNDBN	Xeroderma pigmentosum not provided
Reversed	0
HGVS	NC_000019.9:g.45856059C>G
CLNSRC	Illumina
CLNACC	RCV000312948.1, RCV000489442.1,