rs878854131

Orientation

plus

Stabilized

plus

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

Make rs878854131(-;-)

Make rs878854131(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

31081192

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs878854131
dbSNP (classic)	rs878854131
ClinGen	rs878854131
ebi	rs878854131
HLI	rs878854131
Exac	rs878854131
Gnomad	rs878854131
Varsome	rs878854131
LitVar	rs878854131
Map	rs878854131
PheGenI	rs878854131
Biobank	rs878854131
1000 genomes	rs878854131
hgdp	rs878854131
ensembl	rs878854131
geneview	rs878854131
scholar	rs878854131
google	rs878854131
pharmgkb	rs878854131
gwascentral	rs878854131
openSNP	rs878854131
23andMe	rs878854131
SNPshot	rs878854131
SNPdbe	rs878854131
MSV3d	rs878854131
GWAS Ctlg	rs878854131

Max Magnitude

0

ClinVar
Risk	rs878854131(-;-)
Alt	rs878854131(-;-)
Reference	Rs878854131(A;A)
Significance	Other
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30938708delA
CLNSRC
CLNACC	RCV000232269.3,