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rs387906783

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906783(A;A)
Make rs387906783(A;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17387913
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs387906783
ebirs387906783
HLIrs387906783
Exacrs387906783
Varsomers387906783
Maprs387906783
PheGenIrs387906783
hapmaprs387906783
1000 genomesrs387906783
hgdprs387906783
ensemblrs387906783
gopubmedrs387906783
geneviewrs387906783
scholarrs387906783
googlers387906783
pharmgkbrs387906783
gwascentralrs387906783
openSNPrs387906783
23andMers387906783
23andMe allrs387906783
SNP Nexus

SNPshotrs387906783
SNPdbers387906783
MSV3drs387906783
GWAS Ctlgrs387906783
Max Magnitude0
ClinVar
Risk rs387906783(A;A)
Alt rs387906783(A;A)
Reference Rs387906783(T;T)
Significance Pathogenic
Disease Diabetes mellitus
Variation info
Gene KCNJ11
CLNDBN Diabetes mellitus, permanent neonatal, with neurologic features
Reversed 1
HGVS NC_000011.9:g.17409460A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023046.4,