rs878854136

Orientation

plus

Stabilized

plus

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

Make rs878854136(-;AT)

Make rs878854136(AT;AT)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

31120341

Gene

WRN

is a	snp
is	mentioned by
dbSNP	rs878854136
dbSNP (classic)	rs878854136
ClinGen	rs878854136
ebi	rs878854136
HLI	rs878854136
Exac	rs878854136
Gnomad	rs878854136
Varsome	rs878854136
LitVar	rs878854136
Map	rs878854136
PheGenI	rs878854136
Biobank	rs878854136
1000 genomes	rs878854136
hgdp	rs878854136
ensembl	rs878854136
geneview	rs878854136
scholar	rs878854136
google	rs878854136
pharmgkb	rs878854136
gwascentral	rs878854136
openSNP	rs878854136
23andMe	rs878854136
SNPshot	rs878854136
SNPdbe	rs878854136
MSV3d	rs878854136
GWAS Ctlg	rs878854136

Max Magnitude

0

ClinVar
Risk	rs878854136(TA;TA)
Alt	rs878854136(TA;TA)
Reference	Rs878854136(-;-)
Significance	Pathogenic
Disease	Werner syndrome
Variation	info
Gene	WRN
CLNDBN	Werner syndrome
Reversed	0
HGVS	NC_000008.10:g.30977856_30977857dupAT
CLNSRC
CLNACC	RCV000229897.1,