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rs387906408

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCT;CCT) 0 common in clinvar
Make rs387906408(-;-)
Make rs387906408(-;TCC)
Make rs387906408(TCC;TCC)
ReferenceGRCh38 38.1/141
Chromosome11
Position17395892
GeneABCC8
is asnp
is mentioned by
dbSNPrs387906408
ebirs387906408
HLIrs387906408
Exacrs387906408
Varsomers387906408
Maprs387906408
PheGenIrs387906408
hapmaprs387906408
1000 genomesrs387906408
hgdprs387906408
ensemblrs387906408
gopubmedrs387906408
geneviewrs387906408
scholarrs387906408
googlers387906408
pharmgkbrs387906408
gwascentralrs387906408
openSNPrs387906408
23andMers387906408
23andMe allrs387906408
SNP Nexus

SNPshotrs387906408
SNPdbers387906408
MSV3drs387906408
GWAS Ctlgrs387906408
Max Magnitude0
ClinVar
Risk rs387906408(;)
Alt rs387906408(;)
Reference rs387906408(CCT;CCT)
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.17417439_17417441delGGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000009668.3,