rs876657735

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CTT;CTT)	0	common in clinvar
(TTC;TTC)	0	common in clinvar

Make rs876657735(-;-)

Make rs876657735(-;TTC)

Reference

GRCh38.p2 38.2/147

Chromosome

4

Position

6300855

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs876657735
dbSNP (classic)	rs876657735
ClinGen	rs876657735
ebi	rs876657735
HLI	rs876657735
Exac	rs876657735
Gnomad	rs876657735
Varsome	rs876657735
LitVar	rs876657735
Map	rs876657735
PheGenI	rs876657735
Biobank	rs876657735
1000 genomes	rs876657735
hgdp	rs876657735
ensembl	rs876657735
geneview	rs876657735
scholar	rs876657735
google	rs876657735
pharmgkb	rs876657735
gwascentral	rs876657735
openSNP	rs876657735
23andMe	rs876657735
SNPshot	rs876657735
SNPdbe	rs876657735
MSV3d	rs876657735
GWAS Ctlg	rs876657735

Max Magnitude

0

ClinVar
Risk	rs876657735(-;-) Rs876657735(CTT;CTT)
Alt	rs876657735(-;-) Rs876657735(CTT;CTT)
Reference	Rs876657735(TTC;TTC)
Significance	Pathogenic
Disease	Diabetes mellitus AND insipidus with optic atrophy AND deafness
Variation	info
Gene	WFS1
CLNDBN	Diabetes mellitus AND insipidus with optic atrophy AND deafness
Reversed	0
HGVS	NC_000004.11:g.6302582_6302584delTTC
CLNSRC
CLNACC	RCV000215662.2,