rs121908446

Orientation

plus

Stabilized

plus

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

Make rs121908446(C;T)

Make rs121908446(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

31157461

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs121908446
dbSNP (classic)	rs121908446
ClinGen	rs121908446
ebi	rs121908446
HLI	rs121908446
Exac	rs121908446
Gnomad	rs121908446
Varsome	rs121908446
LitVar	rs121908446
Map	rs121908446
PheGenI	rs121908446
Biobank	rs121908446
1000 genomes	rs121908446
hgdp	rs121908446
ensembl	rs121908446
geneview	rs121908446
scholar	rs121908446
google	rs121908446
pharmgkb	rs121908446
gwascentral	rs121908446
openSNP	rs121908446
23andMe	rs121908446
SNPshot	rs121908446
SNPdbe	rs121908446
MSV3d	rs121908446
GWAS Ctlg	rs121908446

Max Magnitude

0

OMIM	604611
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121908446(T;T)
Alt	rs121908446(T;T)
Reference	Rs121908446(C;C)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.31014977C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005777.2,