rs370454709

Orientation

plus

Stabilized

plus

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

Make rs370454709(C;T)

Make rs370454709(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

45364274

Gene

ERCC2

is a	snp
is	mentioned by
dbSNP	rs370454709
dbSNP (classic)	rs370454709
ClinGen	rs370454709
ebi	rs370454709
HLI	rs370454709
Exac	rs370454709
Gnomad	rs370454709
Varsome	rs370454709
LitVar	rs370454709
Map	rs370454709
PheGenI	rs370454709
Biobank	rs370454709
1000 genomes	rs370454709
hgdp	rs370454709
ensembl	rs370454709
geneview	rs370454709
scholar	rs370454709
google	rs370454709
pharmgkb	rs370454709
gwascentral	rs370454709
openSNP	rs370454709
23andMe	rs370454709
SNPshot	rs370454709
SNPdbe	rs370454709
MSV3d	rs370454709
GWAS Ctlg	rs370454709

Max Magnitude

0

ClinVar
Risk	rs370454709(T;T)
Alt	rs370454709(T;T)
Reference	Rs370454709(C;C)
Significance	Pathogenic
Disease	ERCC2-Related Disorders not provided
Variation	info
Gene	ERCC2
CLNDBN	ERCC2-Related Disorders not provided
Reversed	0
HGVS	NC_000019.9:g.45867532C>T
CLNSRC
CLNACC	RCV000349442.1, RCV000435999.1,