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rs879253757

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879253757(C;T)
Make rs879253757(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position17387938
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs879253757
ebirs879253757
HLIrs879253757
Exacrs879253757
Varsomers879253757
Maprs879253757
PheGenIrs879253757
hapmaprs879253757
1000 genomesrs879253757
hgdprs879253757
ensemblrs879253757
gopubmedrs879253757
geneviewrs879253757
scholarrs879253757
googlers879253757
pharmgkbrs879253757
gwascentralrs879253757
openSNPrs879253757
23andMers879253757
23andMe allrs879253757
SNP Nexus

SNPshotrs879253757
SNPdbers879253757
MSV3drs879253757
GWAS Ctlgrs879253757
Max Magnitude0
ClinVar
Risk rs879253757(T;T)
Alt rs879253757(T;T)
Reference rs879253757(C;C)
Significance Probable-Pathogenic
Disease Islet cell hyperplasia
Variation info
Gene KCNJ11
CLNDBN Islet cell hyperplasia
Reversed 1
HGVS NC_000011.9:g.17409485G>A
CLNSRC University Hospital of Geneva
CLNACC RCV000234886.1,