rs606231162

Orientation

plus

Stabilized

plus

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

Make rs606231162(-;-)

Make rs606231162(-;AGAC)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

31154626

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs606231162
dbSNP (classic)	rs606231162
ClinGen	rs606231162
ebi	rs606231162
HLI	rs606231162
Exac	rs606231162
Gnomad	rs606231162
Varsome	rs606231162
LitVar	rs606231162
Map	rs606231162
PheGenI	rs606231162
Biobank	rs606231162
1000 genomes	rs606231162
hgdp	rs606231162
ensembl	rs606231162
geneview	rs606231162
scholar	rs606231162
google	rs606231162
pharmgkb	rs606231162
gwascentral	rs606231162
openSNP	rs606231162
23andMe	rs606231162
SNPshot	rs606231162
SNPdbe	rs606231162
MSV3d	rs606231162
GWAS Ctlg	rs606231162

Max Magnitude

0

ClinVar
Risk	rs606231162(-;-)
Alt	rs606231162(-;-)
Reference	Rs606231162(AGAC;AGAC)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.31012142_31012145delAGAC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005779.4,