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rs771251369

From SNPedia

Merged intors151344624
Orientationplus
Stabilizedplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs771251369(-;-)
Make rs771251369(-;AGA)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17395888
GeneABCC8
is asnp
is mentioned by
dbSNPrs771251369
dbSNP (old)rs771251369
ClinGenrs771251369
ebirs771251369
HLIrs771251369
Exacrs771251369
Gnomadrs771251369
Varsomers771251369
Maprs771251369
PheGenIrs771251369
Biobankrs771251369
1000 genomesrs771251369
hgdprs771251369
ensemblrs771251369
gopubmedrs771251369
geneviewrs771251369
scholarrs771251369
googlers771251369
pharmgkbrs771251369
gwascentralrs771251369
openSNPrs771251369
23andMers771251369
23andMe allrs771251369
SNP Nexus

SNPshotrs771251369
SNPdbers771251369
MSV3drs771251369
GWAS Ctlgrs771251369
StatusMerged into rs151344624
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs771251369(AGA;AGA)
Significance Pathogenic
Disease Persistent hyperinsulinemic hypoglycemia of infancy not provided
Variation info
Gene ABCC8
CLNDBN Persistent hyperinsulinemic hypoglycemia of infancy not provided
Reversed 0
HGVS NC_000011.9:g.17417435_17417437delAGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000177757.2, RCV000201913.1,