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rs2068330

From SNPedia

Orientationminus
Stabilizedminus
Make rs2068330(C;C)
Make rs2068330(C;G)
Make rs2068330(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position162380880
GeneKCNH7
is asnp
is mentioned by
dbSNPrs2068330
ebirs2068330
HLIrs2068330
Exacrs2068330
Varsomers2068330
Maprs2068330
PheGenIrs2068330
hapmaprs2068330
1000 genomesrs2068330
hgdprs2068330
ensemblrs2068330
gopubmedrs2068330
geneviewrs2068330
scholarrs2068330
googlers2068330
pharmgkbrs2068330
gwascentralrs2068330
openSNPrs2068330
23andMers2068330
23andMe allrs2068330
SNP Nexus

SNPshotrs2068330
SNPdbers2068330
MSV3drs2068330
GWAS Ctlgrs2068330
GMAF0.4174
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 19156166OA-icon.png] A study of 591 French Caucasian multiple sclerosis trio families found no association between rs1990760 or rs2068330 and the disease, which did not confirm one previously reported study.


[PMID 18285833] IFIH1-GCA-KCNH7 locus: influence on multiple sclerosis risk.


[PMID 18927125OA-icon.png] IFIH1 polymorphisms are significantly associated with type 1 diabetes and IFIH1 gene expression in peripheral blood mononuclear cells.


[PMID 19956101OA-icon.png] Overview of the Rapid Response data.


[PMID 19956106OA-icon.png] Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.


[PMID 19956109OA-icon.png] The Type I Diabetes Genetics Consortium 'Rapid Response' family-based candidate gene study: strategy, genes selection, and main outcome.


[PMID 19961590OA-icon.png] The rs1990760 polymorphism within the IFIH1 locus is not associated with Graves' disease, Hashimoto's thyroiditis and Addison's disease.


[PMID 20644636OA-icon.png] Study of transcriptional effects in Cis at the IFIH1 locus.