rs797045076

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(I;I)	0	common genotype
(TCTT;TCTT)	0	common in clinvar
(TTTC;TTTC)	0	common in clinvar

Make rs797045076(-;-)

Make rs797045076(-;TCTT)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

6302443

Gene	LOC107986257, WFS1

is a	snp
is	mentioned by
dbSNP	rs797045076
dbSNP (classic)	rs797045076
ClinGen	rs797045076
ebi	rs797045076
HLI	rs797045076
Exac	rs797045076
Gnomad	rs797045076
Varsome	rs797045076
LitVar	rs797045076
Map	rs797045076
PheGenI	rs797045076
Biobank	rs797045076
1000 genomes	rs797045076
hgdp	rs797045076
ensembl	rs797045076
geneview	rs797045076
scholar	rs797045076
google	rs797045076
pharmgkb	rs797045076
gwascentral	rs797045076
openSNP	rs797045076
23andMe	rs797045076
SNPshot	rs797045076
SNPdbe	rs797045076
MSV3d	rs797045076
GWAS Ctlg	rs797045076

Max Magnitude

0

ClinVar
Risk	rs797045076(-;-) Rs797045076(TTTC;TTTC)
Alt	rs797045076(-;-) Rs797045076(TTTC;TTTC)
Reference	Rs797045076(TCTT;TCTT)
Significance	Pathogenic
Disease	Diabetes mellitus AND insipidus with optic atrophy AND deafness not provided
Variation	info
Gene	WFS1
CLNDBN	Diabetes mellitus AND insipidus with optic atrophy AND deafness not provided
Reversed	0
HGVS	NC_000004.11:g.6304170_6304173delTCTT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000191146.2, RCV000200365.1,