rs775802030

Orientation

plus

Stabilized

plus

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

Make rs775802030(A;G)

Make rs775802030(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

31067089

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs775802030
dbSNP (classic)	rs775802030
ClinGen	rs775802030
ebi	rs775802030
HLI	rs775802030
Exac	rs775802030
Gnomad	rs775802030
Varsome	rs775802030
LitVar	rs775802030
Map	rs775802030
PheGenI	rs775802030
Biobank	rs775802030
1000 genomes	rs775802030
hgdp	rs775802030
ensembl	rs775802030
geneview	rs775802030
scholar	rs775802030
google	rs775802030
pharmgkb	rs775802030
gwascentral	rs775802030
openSNP	rs775802030
23andMe	rs775802030
SNPshot	rs775802030
SNPdbe	rs775802030
MSV3d	rs775802030
GWAS Ctlg	rs775802030

Max Magnitude

0

ClinVar
Risk	rs775802030(G;G)
Alt	rs775802030(G;G)
Reference	Rs775802030(A;A)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30924605A>G
CLNSRC
CLNACC	RCV000179333.1,