rs370324188

Orientation

plus

Stabilized

plus

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

Make rs370324188(C;T)

Make rs370324188(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

31068276

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs370324188
dbSNP (classic)	rs370324188
ClinGen	rs370324188
ebi	rs370324188
HLI	rs370324188
Exac	rs370324188
Gnomad	rs370324188
Varsome	rs370324188
LitVar	rs370324188
Map	rs370324188
PheGenI	rs370324188
Biobank	rs370324188
1000 genomes	rs370324188
hgdp	rs370324188
ensembl	rs370324188
geneview	rs370324188
scholar	rs370324188
google	rs370324188
pharmgkb	rs370324188
gwascentral	rs370324188
openSNP	rs370324188
23andMe	rs370324188
SNPshot	rs370324188
SNPdbe	rs370324188
MSV3d	rs370324188
GWAS Ctlg	rs370324188

Max Magnitude

0

ClinVar
Risk	rs370324188(T;T)
Alt	rs370324188(T;T)
Reference	Rs370324188(C;C)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30925792C>T
CLNSRC
CLNACC	RCV000473494.1,