rs104893881

Orientation

plus

Stabilized

plus

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

Make rs104893881(C;T)

Make rs104893881(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6302250

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs104893881
dbSNP (classic)	rs104893881
ClinGen	rs104893881
ebi	rs104893881
HLI	rs104893881
Exac	rs104893881
Gnomad	rs104893881
Varsome	rs104893881
LitVar	rs104893881
Map	rs104893881
PheGenI	rs104893881
Biobank	rs104893881
1000 genomes	rs104893881
hgdp	rs104893881
ensembl	rs104893881
geneview	rs104893881
scholar	rs104893881
google	rs104893881
pharmgkb	rs104893881
gwascentral	rs104893881
openSNP	rs104893881
23andMe	rs104893881
SNPshot	rs104893881
SNPdbe	rs104893881
MSV3d	rs104893881
GWAS Ctlg	rs104893881

Max Magnitude

0

OMIM	606201
Desc
Variant	0011
Related	also

ClinVar
Risk	rs104893881(T;T)
Alt	rs104893881(T;T)
Reference	Rs104893881(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.6303977C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004775.5,