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rs797045213

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045213(A;G)
Make rs797045213(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17463454
GeneABCC8
is asnp
is mentioned by
dbSNPrs797045213
ebirs797045213
HLIrs797045213
Exacrs797045213
Varsomers797045213
Maprs797045213
PheGenIrs797045213
hapmaprs797045213
1000 genomesrs797045213
hgdprs797045213
ensemblrs797045213
gopubmedrs797045213
geneviewrs797045213
scholarrs797045213
googlers797045213
pharmgkbrs797045213
gwascentralrs797045213
openSNPrs797045213
23andMers797045213
23andMe allrs797045213
SNP Nexus

SNPshotrs797045213
SNPdbers797045213
MSV3drs797045213
GWAS Ctlgrs797045213
Max Magnitude0
ClinVar
Risk rs797045213(G;G)
Alt rs797045213(G;G)
Reference rs797045213(A;A)
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.17485001T>C
CLNSRC
CLNACC RCV000192482.1,