rs121908448

Orientation

plus

Stabilized

plus

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

Make rs121908448(A;T)

Make rs121908448(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

31090843

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs121908448
dbSNP (classic)	rs121908448
ClinGen	rs121908448
ebi	rs121908448
HLI	rs121908448
Exac	rs121908448
Gnomad	rs121908448
Varsome	rs121908448
LitVar	rs121908448
Map	rs121908448
PheGenI	rs121908448
Biobank	rs121908448
1000 genomes	rs121908448
hgdp	rs121908448
ensembl	rs121908448
geneview	rs121908448
scholar	rs121908448
google	rs121908448
pharmgkb	rs121908448
gwascentral	rs121908448
openSNP	rs121908448
23andMe	rs121908448
SNPshot	rs121908448
SNPdbe	rs121908448
MSV3d	rs121908448
GWAS Ctlg	rs121908448

Max Magnitude

0

OMIM	604611
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121908448(T;T)
Alt	rs121908448(T;T)
Reference	Rs121908448(A;A)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30948359A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005785.2,