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rs797045208

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045208(G;G)
Make rs797045208(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17474937
GeneABCC8
is asnp
is mentioned by
dbSNPrs797045208
ebirs797045208
HLIrs797045208
Exacrs797045208
Varsomers797045208
Maprs797045208
PheGenIrs797045208
hapmaprs797045208
1000 genomesrs797045208
hgdprs797045208
ensemblrs797045208
gopubmedrs797045208
geneviewrs797045208
scholarrs797045208
googlers797045208
pharmgkbrs797045208
gwascentralrs797045208
openSNPrs797045208
23andMers797045208
23andMe allrs797045208
SNP Nexus

SNPshotrs797045208
SNPdbers797045208
MSV3drs797045208
GWAS Ctlgrs797045208
Max Magnitude0
ClinVar
Risk rs797045208(G;G)
Alt rs797045208(G;G)
Reference rs797045208(T;T)
Significance Probable-Pathogenic
Disease Persistent hyperinsulinemic hypoglycemia of infancy
Variation info
Gene ABCC8
CLNDBN Persistent hyperinsulinemic hypoglycemia of infancy
Reversed 1
HGVS NC_000011.9:g.17496484A>C
CLNSRC
CLNACC RCV000192892.1,