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rs797045206

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045206(C;C)
Make rs797045206(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17442818
GeneABCC8
is asnp
is mentioned by
dbSNPrs797045206
ebirs797045206
HLIrs797045206
Exacrs797045206
Varsomers797045206
Maprs797045206
PheGenIrs797045206
hapmaprs797045206
1000 genomesrs797045206
hgdprs797045206
ensemblrs797045206
gopubmedrs797045206
geneviewrs797045206
scholarrs797045206
googlers797045206
pharmgkbrs797045206
gwascentralrs797045206
openSNPrs797045206
23andMers797045206
23andMe allrs797045206
SNP Nexus

SNPshotrs797045206
SNPdbers797045206
MSV3drs797045206
GWAS Ctlgrs797045206
Max Magnitude0
ClinVar
Risk rs797045206(C;C)
Alt rs797045206(C;C)
Reference rs797045206(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.17464365A>G
CLNSRC
CLNACC RCV000194750.1,