rs587776621

Orientation

plus

Stabilized

plus

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

Make rs587776621(-;A)

Make rs587776621(A;A)

Reference

GRCh38 38.1/142

Chromosome

8

Position

31157463

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs587776621
dbSNP (classic)	rs587776621
ClinGen	rs587776621
ebi	rs587776621
HLI	rs587776621
Exac	rs587776621
Gnomad	rs587776621
Varsome	rs587776621
LitVar	rs587776621
Map	rs587776621
PheGenI	rs587776621
Biobank	rs587776621
1000 genomes	rs587776621
hgdp	rs587776621
ensembl	rs587776621
geneview	rs587776621
scholar	rs587776621
google	rs587776621
pharmgkb	rs587776621
gwascentral	rs587776621
openSNP	rs587776621
23andMe	rs587776621
SNPshot	rs587776621
SNPdbe	rs587776621
MSV3d	rs587776621
GWAS Ctlg	rs587776621

Max Magnitude

0

ClinVar
Risk	rs587776621(A;A)
Alt	rs587776621(A;A)
Reference	Rs587776621(-;-)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.31014979dupA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005781.2,