rs747319628

Orientation

plus

Stabilized

plus

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

Make rs747319628(C;T)

Make rs747319628(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

8

Position

31132498

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs747319628
dbSNP (classic)	rs747319628
ClinGen	rs747319628
ebi	rs747319628
HLI	rs747319628
Exac	rs747319628
Gnomad	rs747319628
Varsome	rs747319628
LitVar	rs747319628
Map	rs747319628
PheGenI	rs747319628
Biobank	rs747319628
1000 genomes	rs747319628
hgdp	rs747319628
ensembl	rs747319628
geneview	rs747319628
scholar	rs747319628
google	rs747319628
pharmgkb	rs747319628
gwascentral	rs747319628
openSNP	rs747319628
23andMe	rs747319628
SNPshot	rs747319628
SNPdbe	rs747319628
MSV3d	rs747319628
GWAS Ctlg	rs747319628

Max Magnitude

0

ClinVar
Risk	rs747319628(T;T)
Alt	rs747319628(T;T)
Reference	Rs747319628(C;C)
Significance	Probable-Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30990014C>T
CLNSRC	Illumina
CLNACC	RCV000269754.1,