rs6446482

plus

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

Make rs6446482(C;G)

Make rs6446482(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6293966

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs6446482
dbSNP (classic)	rs6446482
ClinGen	rs6446482
ebi	rs6446482
HLI	rs6446482
Exac	rs6446482
Gnomad	rs6446482
Varsome	rs6446482
LitVar	rs6446482
Map	rs6446482
PheGenI	rs6446482
Biobank	rs6446482
1000 genomes	rs6446482
hgdp	rs6446482
ensembl	rs6446482
geneview	rs6446482
scholar	rs6446482
google	rs6446482
pharmgkb	rs6446482
gwascentral	rs6446482
openSNP	rs6446482
23andMe	rs6446482
SNPshot	rs6446482
SNPdbe	rs6446482
MSV3d	rs6446482
GWAS Ctlg	rs6446482

GMAF

0.2741

Max Magnitude

0

?

(C;C) (C;G) (G;G)

28

[PMID 19258739] Association study of the effect of WFS1 polymorphisms on risk of type 2 diabetes in Japanese population

OMIM	125853
Desc	DIABETES MELLITUS, NONINSULIN-DEPENDENT; NIDDM
Variant
Related	also

OMIM	606201
Desc	WFS1 GENE; WFS1
Variant
Related	also

OMIM	606201
Desc
Variant	0021
Related	also

OMIM	606201
Desc
Variant	0022
Related	also

[PMID 18040659 ] Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations.

[PMID 18060660 ] Testing of diabetes-associated WFS1 polymorphisms in the Diabetes Prevention Program.

[PMID 20509872 ] Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population.

[PMID 22996131 ] Monogenic models: what have the single gene disorders taught us?

ClinVar
Risk	rs6446482(G;G)
Alt	rs6446482(G;G)
Reference	Rs6446482(C;C)
Significance	Pathogenic
Disease	Diabetes mellitus
Variation	info
Gene	WFS1
CLNDBN	Diabetes mellitus, noninsulin-dependent, association with
Reversed	0
HGVS	NC_000004.11:g.6295693C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004786.7,