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rs387906398

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906398(G;T)
Make rs387906398(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17388225
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs387906398
ebirs387906398
HLIrs387906398
Exacrs387906398
Varsomers387906398
Maprs387906398
PheGenIrs387906398
hapmaprs387906398
1000 genomesrs387906398
hgdprs387906398
ensemblrs387906398
gopubmedrs387906398
geneviewrs387906398
scholarrs387906398
googlers387906398
pharmgkbrs387906398
gwascentralrs387906398
openSNPrs387906398
23andMers387906398
23andMe allrs387906398
SNP Nexus

SNPshotrs387906398
SNPdbers387906398
MSV3drs387906398
GWAS Ctlgrs387906398
Max Magnitude0
ClinVar
Risk rs387906398(T;T)
Alt rs387906398(T;T)
Reference rs387906398(G;G)
Significance Pathogenic
Disease Islet cell hyperplasia
Variation info
Gene KCNJ11
CLNDBN Islet cell hyperplasia
Reversed 1
HGVS NC_000011.9:g.17409772C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009209.3,