rs121908447

Orientation

plus

Stabilized

plus

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

Make rs121908447(C;T)

Make rs121908447(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

31147397

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs121908447
dbSNP (classic)	rs121908447
ClinGen	rs121908447
ebi	rs121908447
HLI	rs121908447
Exac	rs121908447
Gnomad	rs121908447
Varsome	rs121908447
LitVar	rs121908447
Map	rs121908447
PheGenI	rs121908447
Biobank	rs121908447
1000 genomes	rs121908447
hgdp	rs121908447
ensembl	rs121908447
geneview	rs121908447
scholar	rs121908447
google	rs121908447
pharmgkb	rs121908447
gwascentral	rs121908447
openSNP	rs121908447
23andMe	rs121908447
SNPshot	rs121908447
SNPdbe	rs121908447
MSV3d	rs121908447
GWAS Ctlg	rs121908447

Max Magnitude

0

OMIM	604611
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908447(T;T)
Alt	rs121908447(T;T)
Reference	Rs121908447(C;C)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.31004913C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005778.3,