Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204717

From SNPedia

Orientationminus
Geno Mag Summary
(GACT;GACT) 0 common in clinvar
Make rs786204717(-;-)
Make rs786204717(-;GACT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17427144
GeneABCC8
is asnp
is mentioned by
dbSNPrs786204717
ebirs786204717
HLIrs786204717
Exacrs786204717
Varsomers786204717
Maprs786204717
PheGenIrs786204717
hapmaprs786204717
1000 genomesrs786204717
hgdprs786204717
ensemblrs786204717
gopubmedrs786204717
geneviewrs786204717
scholarrs786204717
googlers786204717
pharmgkbrs786204717
gwascentralrs786204717
openSNPrs786204717
23andMers786204717
23andMe allrs786204717
SNP Nexus

SNPshotrs786204717
SNPdbers786204717
MSV3drs786204717
GWAS Ctlgrs786204717
Max Magnitude0
ClinVar
Risk rs786204717(;)
Alt rs786204717(;)
Reference rs786204717(GACT;GACT)
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.17448691_17448694delAGTC
CLNSRC Counsyl
CLNACC RCV000169534.1,