rs281865160

Orientation

plus

Stabilized

plus

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

Make rs281865160(-;-)

Make rs281865160(-;A)

Reference

GRCh38 38.1/141

Chromosome

8

Position

31150358

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs281865160
dbSNP (classic)	rs281865160
ClinGen	rs281865160
ebi	rs281865160
HLI	rs281865160
Exac	rs281865160
Gnomad	rs281865160
Varsome	rs281865160
LitVar	rs281865160
Map	rs281865160
PheGenI	rs281865160
Biobank	rs281865160
1000 genomes	rs281865160
hgdp	rs281865160
ensembl	rs281865160
geneview	rs281865160
scholar	rs281865160
google	rs281865160
pharmgkb	rs281865160
gwascentral	rs281865160
openSNP	rs281865160
23andMe	rs281865160
SNPshot	rs281865160
SNPdbe	rs281865160
MSV3d	rs281865160
GWAS Ctlg	rs281865160

Max Magnitude

0

ClinVar
Risk	rs281865160(-;-)
Alt	rs281865160(-;-)
Reference	Rs281865160(A;A)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.31007874delA
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000032139.1,

[PMID 20443122] WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.