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rs786204676

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204676(C;C)
Make rs786204676(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17427865
GeneABCC8
is asnp
is mentioned by
dbSNPrs786204676
ebirs786204676
HLIrs786204676
Exacrs786204676
Varsomers786204676
Maprs786204676
PheGenIrs786204676
hapmaprs786204676
1000 genomesrs786204676
hgdprs786204676
ensemblrs786204676
gopubmedrs786204676
geneviewrs786204676
scholarrs786204676
googlers786204676
pharmgkbrs786204676
gwascentralrs786204676
openSNPrs786204676
23andMers786204676
23andMe allrs786204676
SNP Nexus

SNPshotrs786204676
SNPdbers786204676
MSV3drs786204676
GWAS Ctlgrs786204676
Max Magnitude0
ClinVar
Risk rs786204676(C;C)
Alt rs786204676(C;C)
Reference rs786204676(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.17449412A>G
CLNSRC Counsyl
CLNACC RCV000169482.1,