rs146670741

Orientation

plus

Stabilized

plus

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

Make rs146670741(A;A)

Make rs146670741(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

6301681

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs146670741
dbSNP (classic)	rs146670741
ClinGen	rs146670741
ebi	rs146670741
HLI	rs146670741
Exac	rs146670741
Gnomad	rs146670741
Varsome	rs146670741
LitVar	rs146670741
Map	rs146670741
PheGenI	rs146670741
Biobank	rs146670741
1000 genomes	rs146670741
hgdp	rs146670741
ensembl	rs146670741
geneview	rs146670741
scholar	rs146670741
google	rs146670741
pharmgkb	rs146670741
gwascentral	rs146670741
openSNP	rs146670741
23andMe	rs146670741
SNPshot	rs146670741
SNPdbe	rs146670741
MSV3d	rs146670741
GWAS Ctlg	rs146670741

Max Magnitude

0

ClinVar
Risk	rs146670741(A;A)
Alt	rs146670741(A;A)
Reference	Rs146670741(G;G)
Significance	Probable-Pathogenic
Disease	WFS1-Related Disorders not specified
Variation	info
Gene	WFS1
CLNDBN	WFS1-Related Disorders not specified
Reversed	0
HGVS	NC_000004.11:g.6303408G>A
CLNSRC
CLNACC	RCV000038647.2, RCV000196272.1,