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rs761749884

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761749884(C;T)
Make rs761749884(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17470182
GeneABCC8
is asnp
is mentioned by
dbSNPrs761749884
ebirs761749884
HLIrs761749884
Exacrs761749884
Varsomers761749884
Maprs761749884
PheGenIrs761749884
hapmaprs761749884
1000 genomesrs761749884
hgdprs761749884
ensemblrs761749884
gopubmedrs761749884
geneviewrs761749884
scholarrs761749884
googlers761749884
pharmgkbrs761749884
gwascentralrs761749884
openSNPrs761749884
23andMers761749884
23andMe allrs761749884
SNP Nexus

SNPshotrs761749884
SNPdbers761749884
MSV3drs761749884
GWAS Ctlgrs761749884
Max Magnitude0
ClinVar
Risk rs761749884(T;T)
Alt rs761749884(T;T)
Reference rs761749884(C;C)
Significance Pathogenic
Disease Persistent hyperinsulinemic hypoglycemia of infancy
Variation info
Gene ABCC8
CLNDBN Persistent hyperinsulinemic hypoglycemia of infancy
Reversed 0
HGVS NC_000011.9:g.17491729C>T
CLNSRC
CLNACC RCV000193936.1,