rs1801214

Orientation

plus

Stabilized

plus

Make rs1801214(C;C)

Make rs1801214(C;T)

Make rs1801214(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6301295

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs1801214
dbSNP (classic)	rs1801214
ClinGen	rs1801214
ebi	rs1801214
HLI	rs1801214
Exac	rs1801214
Gnomad	rs1801214
Varsome	rs1801214
LitVar	rs1801214
Map	rs1801214
PheGenI	rs1801214
Biobank	rs1801214
1000 genomes	rs1801214
hgdp	rs1801214
ensembl	rs1801214
geneview	rs1801214
scholar	rs1801214
google	rs1801214
pharmgkb	rs1801214
gwascentral	rs1801214
openSNP	rs1801214
23andMe	rs1801214
SNPshot	rs1801214
SNPdbe	rs1801214
MSV3d	rs1801214
GWAS Ctlg	rs1801214

GMAF

0.2677

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 20581827]
Trait	Type 2 diabetes
Title	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Risk Allele	T
P-val	3E-8
Odds Ratio	1.13 [1.08-1.18]

[PMID 23462794] Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets.

ClinVar
Risk	rs1801214(A;A) rs1801214(G;G) rs1801214(T;T)
Alt	rs1801214(A;A) rs1801214(G;G) rs1801214(T;T)
Reference	rs1801214(C;C)
Significance	Other
Disease	not specified Nonsyndromic Hearing Loss WFS1-Related Spectrum Disorders
Variation	info
Gene	WFS1
CLNDBN	not specified Nonsyndromic Hearing Loss, Dominant WFS1-Related Spectrum Disorders
Reversed	0
HGVS	NC_000004.11:g.6303022C>T
CLNSRC	ClinVar Emory University University of Chicago
CLNACC	RCV000038641.10, RCV000294241.1, RCV000330600.1,

[PMID 29988211] Association of CpG-SNP and 3'UTR-SNP of WFS1 with the Risk of Type 2 Diabetes Mellitus in an Iranian Population.