rs1060500056

Orientation

plus

Stabilized

plus

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

Make rs1060500056(-;-)

Make rs1060500056(-;AA)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

31065061

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs1060500056
dbSNP (classic)	rs1060500056
ClinGen	rs1060500056
ebi	rs1060500056
HLI	rs1060500056
Exac	rs1060500056
Gnomad	rs1060500056
Varsome	rs1060500056
LitVar	rs1060500056
Map	rs1060500056
PheGenI	rs1060500056
Biobank	rs1060500056
1000 genomes	rs1060500056
hgdp	rs1060500056
ensembl	rs1060500056
geneview	rs1060500056
scholar	rs1060500056
google	rs1060500056
pharmgkb	rs1060500056
gwascentral	rs1060500056
openSNP	rs1060500056
23andMe	rs1060500056
SNPshot	rs1060500056
SNPdbe	rs1060500056
MSV3d	rs1060500056
GWAS Ctlg	rs1060500056

Max Magnitude

0

ClinVar
Risk	rs1060500056(-;-)
Alt	rs1060500056(-;-)
Reference	Rs1060500056(AA;AA)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30922577_30922578delAA
CLNSRC
CLNACC	RCV000472438.1,