rs797045118

Orientation

plus

Stabilized

plus

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

Make rs797045118(-;-)

Make rs797045118(-;GA)

Make rs797045118(GA;GA)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

31065046

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs797045118
dbSNP (classic)	rs797045118
ClinGen	rs797045118
ebi	rs797045118
HLI	rs797045118
Exac	rs797045118
Gnomad	rs797045118
Varsome	rs797045118
LitVar	rs797045118
Map	rs797045118
PheGenI	rs797045118
Biobank	rs797045118
1000 genomes	rs797045118
hgdp	rs797045118
ensembl	rs797045118
geneview	rs797045118
scholar	rs797045118
google	rs797045118
pharmgkb	rs797045118
gwascentral	rs797045118
openSNP	rs797045118
23andMe	rs797045118
SNPshot	rs797045118
SNPdbe	rs797045118
MSV3d	rs797045118
GWAS Ctlg	rs797045118

Max Magnitude

0

ClinVar
Risk	rs797045118(-;-)
Alt	rs797045118(-;-)
Reference	Rs797045118(AG;AG)
Significance	Probable-Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30922562_30922563delGA
CLNSRC
CLNACC	RCV000190647.1,