rs774765029

Orientation

plus

Stabilized

plus

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

Make rs774765029(C;T)

Make rs774765029(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

31124556

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs774765029
dbSNP (classic)	rs774765029
ClinGen	rs774765029
ebi	rs774765029
HLI	rs774765029
Exac	rs774765029
Gnomad	rs774765029
Varsome	rs774765029
LitVar	rs774765029
Map	rs774765029
PheGenI	rs774765029
Biobank	rs774765029
1000 genomes	rs774765029
hgdp	rs774765029
ensembl	rs774765029
geneview	rs774765029
scholar	rs774765029
google	rs774765029
pharmgkb	rs774765029
gwascentral	rs774765029
openSNP	rs774765029
23andMe	rs774765029
SNPshot	rs774765029
SNPdbe	rs774765029
MSV3d	rs774765029
GWAS Ctlg	rs774765029

Max Magnitude

0

ClinVar
Risk	rs774765029(T;T)
Alt	rs774765029(T;T)
Reference	Rs774765029(C;C)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30982072C>T
CLNSRC
CLNACC	RCV000456191.1,