rs773359656

Orientation

plus

Stabilized

plus

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

Make rs773359656(A;A)

Make rs773359656(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

45352646

Gene

ERCC2

is a	snp
is	mentioned by
dbSNP	rs773359656
dbSNP (classic)	rs773359656
ClinGen	rs773359656
ebi	rs773359656
HLI	rs773359656
Exac	rs773359656
Gnomad	rs773359656
Varsome	rs773359656
LitVar	rs773359656
Map	rs773359656
PheGenI	rs773359656
Biobank	rs773359656
1000 genomes	rs773359656
hgdp	rs773359656
ensembl	rs773359656
geneview	rs773359656
scholar	rs773359656
google	rs773359656
pharmgkb	rs773359656
gwascentral	rs773359656
openSNP	rs773359656
23andMe	rs773359656
SNPshot	rs773359656
SNPdbe	rs773359656
MSV3d	rs773359656
GWAS Ctlg	rs773359656

Max Magnitude

0

ClinVar
Risk	rs773359656(A;A)
Alt	rs773359656(A;A)
Reference	Rs773359656(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ERCC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.45855904G>A
CLNSRC
CLNACC	RCV000494513.1,