rs267607008

Orientation

plus

Stabilized

plus

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

Make rs267607008(A;G)

Make rs267607008(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

31064962

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs267607008
dbSNP (classic)	rs267607008
ClinGen	rs267607008
ebi	rs267607008
HLI	rs267607008
Exac	rs267607008
Gnomad	rs267607008
Varsome	rs267607008
LitVar	rs267607008
Map	rs267607008
PheGenI	rs267607008
Biobank	rs267607008
1000 genomes	rs267607008
hgdp	rs267607008
ensembl	rs267607008
geneview	rs267607008
scholar	rs267607008
google	rs267607008
pharmgkb	rs267607008
gwascentral	rs267607008
openSNP	rs267607008
23andMe	rs267607008
SNPshot	rs267607008
SNPdbe	rs267607008
MSV3d	rs267607008
GWAS Ctlg	rs267607008

Max Magnitude

0

ClinVar
Risk	rs267607008(G;G)
Alt	rs267607008(G;G)
Reference	Rs267607008(A;A)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30922478A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005786.2,