rs777580652

Orientation

plus

Stabilized

plus

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

Make rs777580652(C;T)

Make rs777580652(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

6300668

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs777580652
dbSNP (classic)	rs777580652
ClinGen	rs777580652
ebi	rs777580652
HLI	rs777580652
Exac	rs777580652
Gnomad	rs777580652
Varsome	rs777580652
LitVar	rs777580652
Map	rs777580652
PheGenI	rs777580652
Biobank	rs777580652
1000 genomes	rs777580652
hgdp	rs777580652
ensembl	rs777580652
geneview	rs777580652
scholar	rs777580652
google	rs777580652
pharmgkb	rs777580652
gwascentral	rs777580652
openSNP	rs777580652
23andMe	rs777580652
SNPshot	rs777580652
SNPdbe	rs777580652
MSV3d	rs777580652
GWAS Ctlg	rs777580652

Max Magnitude

0

ClinVar
Risk	rs777580652(G;G) rs777580652(T;T)
Alt	rs777580652(G;G) rs777580652(T;T)
Reference	Rs777580652(C;C)
Significance	Pathogenic
Disease	Wolfram syndrome
Variation	info
Gene	WFS1
CLNDBN	Wolfram syndrome
Reversed	0
HGVS	NC_000004.11:g.6302395C>G
CLNSRC
CLNACC	RCV000192573.1,