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rs1800467

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1800467(C;G)
Make rs1800467(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position17387284
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs1800467
ebirs1800467
HLIrs1800467
Exacrs1800467
Varsomers1800467
Maprs1800467
PheGenIrs1800467
hapmaprs1800467
1000 genomesrs1800467
hgdprs1800467
ensemblrs1800467
gopubmedrs1800467
geneviewrs1800467
scholarrs1800467
googlers1800467
pharmgkbrs1800467
gwascentralrs1800467
openSNPrs1800467
23andMers1800467
23andMe allrs1800467
SNP Nexus

SNPshotrs1800467
SNPdbers1800467
MSV3drs1800467
GWAS Ctlgrs1800467
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 25247988OA-icon.png] Population Specific Impact of Genetic Variants in KCNJ11 Gene to Type 2 Diabetes: A Case-Control and Meta-Analysis Study


ClinVar
Risk rs1800467(A,G;A,G)
Alt rs1800467(A,G;A,G)
Reference rs1800467(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene KCNJ11
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.17408831G>C
CLNSRC ClinVar University of Chicago
CLNACC RCV000146119.1,



[PMID 25733456] Genetic Variations in Magnesium-Related Ion Channels May Affect Diabetes Risk among African American and Hispanic American Women