rs772319506

Orientation

plus

Stabilized

plus

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

Make rs772319506(G;G)

Make rs772319506(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

31091900

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs772319506
dbSNP (classic)	rs772319506
ClinGen	rs772319506
ebi	rs772319506
HLI	rs772319506
Exac	rs772319506
Gnomad	rs772319506
Varsome	rs772319506
LitVar	rs772319506
Map	rs772319506
PheGenI	rs772319506
Biobank	rs772319506
1000 genomes	rs772319506
hgdp	rs772319506
ensembl	rs772319506
geneview	rs772319506
scholar	rs772319506
google	rs772319506
pharmgkb	rs772319506
gwascentral	rs772319506
openSNP	rs772319506
23andMe	rs772319506
SNPshot	rs772319506
SNPdbe	rs772319506
MSV3d	rs772319506
GWAS Ctlg	rs772319506

Max Magnitude

0

ClinVar
Risk	rs772319506(G;G)
Alt	rs772319506(G;G)
Reference	Rs772319506(T;T)
Significance	Probable-Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30949416T>G
CLNSRC
CLNACC	RCV000471062.1,