Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906407

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906407(A;A)
Make rs387906407(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position17395610
GeneABCC8
is asnp
is mentioned by
dbSNPrs387906407
ebirs387906407
HLIrs387906407
Exacrs387906407
Varsomers387906407
Maprs387906407
PheGenIrs387906407
hapmaprs387906407
1000 genomesrs387906407
hgdprs387906407
ensemblrs387906407
gopubmedrs387906407
geneviewrs387906407
scholarrs387906407
googlers387906407
pharmgkbrs387906407
gwascentralrs387906407
openSNPrs387906407
23andMers387906407
23andMe allrs387906407
SNP Nexus

SNPshotrs387906407
SNPdbers387906407
MSV3drs387906407
GWAS Ctlgrs387906407
Max Magnitude0
ClinVar
Risk rs387906407(A;A)
Alt rs387906407(A;A)
Reference rs387906407(G;G)
Significance Pathogenic
Disease Persistent hyperinsulinemic hypoglycemia of infancy
Variation info
Gene ABCC8
CLNDBN Persistent hyperinsulinemic hypoglycemia of infancy
Reversed 1
HGVS NC_000011.9:g.17417157C>T
CLNSRC OMIM Allelic Variant Sequence Ontology
CLNACC RCV000009654.4,