rs863224262

Orientation

plus

Stabilized

plus

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

Make rs863224262(G;G)

Make rs863224262(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

6302377

Gene	LOC107986257, WFS1

is a	snp
is	mentioned by
dbSNP	rs863224262
dbSNP (classic)	rs863224262
ClinGen	rs863224262
ebi	rs863224262
HLI	rs863224262
Exac	rs863224262
Gnomad	rs863224262
Varsome	rs863224262
LitVar	rs863224262
Map	rs863224262
PheGenI	rs863224262
Biobank	rs863224262
1000 genomes	rs863224262
hgdp	rs863224262
ensembl	rs863224262
geneview	rs863224262
scholar	rs863224262
google	rs863224262
pharmgkb	rs863224262
gwascentral	rs863224262
openSNP	rs863224262
23andMe	rs863224262
SNPshot	rs863224262
SNPdbe	rs863224262
MSV3d	rs863224262
GWAS Ctlg	rs863224262

Max Magnitude

0

ClinVar
Risk	rs863224262(G;G)
Alt	rs863224262(G;G)
Reference	Rs863224262(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	WFS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.6304104T>G
CLNSRC
CLNACC	RCV000197483.1,