rs863224268

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CT;CT)	0	common in clinvar
(I;I)	0	common genotype
(TC;TC)	0	common in clinvar

Make rs863224268(-;-)

Make rs863224268(-;CT)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

6302438

Gene	LOC107986257, WFS1

is a	snp
is	mentioned by
dbSNP	rs863224268
dbSNP (classic)	rs863224268
ClinGen	rs863224268
ebi	rs863224268
HLI	rs863224268
Exac	rs863224268
Gnomad	rs863224268
Varsome	rs863224268
LitVar	rs863224268
Map	rs863224268
PheGenI	rs863224268
Biobank	rs863224268
1000 genomes	rs863224268
hgdp	rs863224268
ensembl	rs863224268
geneview	rs863224268
scholar	rs863224268
google	rs863224268
pharmgkb	rs863224268
gwascentral	rs863224268
openSNP	rs863224268
23andMe	rs863224268
SNPshot	rs863224268
SNPdbe	rs863224268
MSV3d	rs863224268
GWAS Ctlg	rs863224268

Max Magnitude

0

ClinVar
Risk	rs863224268(-;-) Rs863224268(TC;TC)
Alt	rs863224268(-;-) Rs863224268(TC;TC)
Reference	Rs863224268(CT;CT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	WFS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.6304165_6304166delCT
CLNSRC
CLNACC	RCV000199613.1,