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rs151344623

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151344623(A;A)
Make rs151344623(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position17397055
GeneABCC8
is asnp
is mentioned by
dbSNPrs151344623
ebirs151344623
HLIrs151344623
Exacrs151344623
Varsomers151344623
Maprs151344623
PheGenIrs151344623
hapmaprs151344623
1000 genomesrs151344623
hgdprs151344623
ensemblrs151344623
gopubmedrs151344623
geneviewrs151344623
scholarrs151344623
googlers151344623
pharmgkbrs151344623
gwascentralrs151344623
openSNPrs151344623
23andMers151344623
23andMe allrs151344623
SNP Nexus

SNPshotrs151344623
SNPdbers151344623
MSV3drs151344623
GWAS Ctlgrs151344623
Max Magnitude0
OMIM600509
Desc
Variant0002
Relatedalso
ClinVar
Risk rs151344623(A,C;A,C)
Alt rs151344623(A,C;A,C)
Reference rs151344623(G;G)
Significance Pathogenic
Disease Persistent hyperinsulinemic hypoglycemia of infancy not provided
Variation info
Gene ABCC8
CLNDBN Persistent hyperinsulinemic hypoglycemia of infancy not provided
Reversed 1
HGVS NC_000011.9:g.17418602C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009656.4, RCV000144995.1,