rs369158322

Orientation

plus

Stabilized

plus

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

Make rs369158322(A;C)

Make rs369158322(C;C)

Reference

GRCh38 38.1/142

Chromosome

8

Position

31150454

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs369158322
dbSNP (classic)	rs369158322
ClinGen	rs369158322
ebi	rs369158322
HLI	rs369158322
Exac	rs369158322
Gnomad	rs369158322
Varsome	rs369158322
LitVar	rs369158322
Map	rs369158322
PheGenI	rs369158322
Biobank	rs369158322
1000 genomes	rs369158322
hgdp	rs369158322
ensembl	rs369158322
geneview	rs369158322
scholar	rs369158322
google	rs369158322
pharmgkb	rs369158322
gwascentral	rs369158322
openSNP	rs369158322
23andMe	rs369158322
SNPshot	rs369158322
SNPdbe	rs369158322
MSV3d	rs369158322
GWAS Ctlg	rs369158322

Max Magnitude

0

ClinVar
Risk	rs369158322(C;C) rs369158322(T;T)
Alt	rs369158322(C;C) rs369158322(T;T)
Reference	Rs369158322(A;A)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.31007970A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005783.3,