rs387906337

Orientation

plus

Stabilized

plus

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

Make rs387906337(A;T)

Make rs387906337(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

31064934

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs387906337
dbSNP (classic)	rs387906337
ClinGen	rs387906337
ebi	rs387906337
HLI	rs387906337
Exac	rs387906337
Gnomad	rs387906337
Varsome	rs387906337
LitVar	rs387906337
Map	rs387906337
PheGenI	rs387906337
Biobank	rs387906337
1000 genomes	rs387906337
hgdp	rs387906337
ensembl	rs387906337
geneview	rs387906337
scholar	rs387906337
google	rs387906337
pharmgkb	rs387906337
gwascentral	rs387906337
openSNP	rs387906337
23andMe	rs387906337
SNPshot	rs387906337
SNPdbe	rs387906337
MSV3d	rs387906337
GWAS Ctlg	rs387906337

Max Magnitude

0

ClinVar
Risk	rs387906337(T;T)
Alt	rs387906337(T;T)
Reference	Rs387906337(A;A)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30922450A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005786.2,