rs878854133

Orientation

plus

Stabilized

plus

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

Make rs878854133(-;-)

Make rs878854133(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

31058462

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs878854133
dbSNP (classic)	rs878854133
ClinGen	rs878854133
ebi	rs878854133
HLI	rs878854133
Exac	rs878854133
Gnomad	rs878854133
Varsome	rs878854133
LitVar	rs878854133
Map	rs878854133
PheGenI	rs878854133
Biobank	rs878854133
1000 genomes	rs878854133
hgdp	rs878854133
ensembl	rs878854133
geneview	rs878854133
scholar	rs878854133
google	rs878854133
pharmgkb	rs878854133
gwascentral	rs878854133
openSNP	rs878854133
23andMe	rs878854133
SNPshot	rs878854133
SNPdbe	rs878854133
MSV3d	rs878854133
GWAS Ctlg	rs878854133

Max Magnitude

0

ClinVar
Risk	rs878854133(-;-)
Alt	rs878854133(-;-)
Reference	Rs878854133(A;A)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30915978delA
CLNSRC
CLNACC	RCV000233160.1,