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rs1801214

From SNPedia

Orientationplus
Stabilizedplus
Make rs1801214(C;C)
Make rs1801214(C;T)
Make rs1801214(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position6301295
GeneWFS1
is asnp
is mentioned by
dbSNPrs1801214
dbSNP (classic)rs1801214
ClinGenrs1801214
ebirs1801214
HLIrs1801214
Exacrs1801214
Gnomadrs1801214
Varsomers1801214
LitVarrs1801214
Maprs1801214
PheGenIrs1801214
Biobankrs1801214
1000 genomesrs1801214
hgdprs1801214
ensemblrs1801214
geneviewrs1801214
scholarrs1801214
googlers1801214
pharmgkbrs1801214
gwascentralrs1801214
openSNPrs1801214
23andMers1801214
SNPshotrs1801214
SNPdbers1801214
MSV3drs1801214
GWAS Ctlgrs1801214
GMAF0.2677
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 20581827OA-icon.png]
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 23462794OA-icon.png] 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 29988211OA-icon.png] Association of CpG-SNP and 3'UTR-SNP of WFS1 with the Risk of Type 2 Diabetes Mellitus in an Iranian Population.