rs28937892

Orientation

plus

Stabilized

plus

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

Make rs28937892(C;T)

Make rs28937892(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6301306

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs28937892
dbSNP (classic)	rs28937892
ClinGen	rs28937892
ebi	rs28937892
HLI	rs28937892
Exac	rs28937892
Gnomad	rs28937892
Varsome	rs28937892
LitVar	rs28937892
Map	rs28937892
PheGenI	rs28937892
Biobank	rs28937892
1000 genomes	rs28937892
hgdp	rs28937892
ensembl	rs28937892
geneview	rs28937892
scholar	rs28937892
google	rs28937892
pharmgkb	rs28937892
gwascentral	rs28937892
openSNP	rs28937892
23andMe	rs28937892
SNPshot	rs28937892
SNPdbe	rs28937892
MSV3d	rs28937892
GWAS Ctlg	rs28937892

Max Magnitude

0

OMIM	606201
Desc	WOLFRAM SYNDROME
Variant	0006
Related	also

ClinVar
Risk	rs28937892(T;T)
Alt	rs28937892(T;T)
Reference	Rs28937892(C;C)
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.6303033C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004770.3,