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rs797045207

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045207(A;A)
Make rs797045207(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17427155
GeneABCC8
is asnp
is mentioned by
dbSNPrs797045207
ebirs797045207
HLIrs797045207
Exacrs797045207
Varsomers797045207
Maprs797045207
PheGenIrs797045207
hapmaprs797045207
1000 genomesrs797045207
hgdprs797045207
ensemblrs797045207
gopubmedrs797045207
geneviewrs797045207
scholarrs797045207
googlers797045207
pharmgkbrs797045207
gwascentralrs797045207
openSNPrs797045207
23andMers797045207
23andMe allrs797045207
SNP Nexus

SNPshotrs797045207
SNPdbers797045207
MSV3drs797045207
GWAS Ctlgrs797045207
Max Magnitude0
ClinVar
Risk rs797045207(A;A)
Alt rs797045207(A;A)
Reference rs797045207(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.17448702C>T
CLNSRC
CLNACC RCV000194857.1,