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rs587783169

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783169(-;-)
Make rs587783169(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position17404560
GeneABCC8
is asnp
is mentioned by
dbSNPrs587783169
ebirs587783169
HLIrs587783169
Exacrs587783169
Varsomers587783169
Maprs587783169
PheGenIrs587783169
hapmaprs587783169
1000 genomesrs587783169
hgdprs587783169
ensemblrs587783169
gopubmedrs587783169
geneviewrs587783169
scholarrs587783169
googlers587783169
pharmgkbrs587783169
gwascentralrs587783169
openSNPrs587783169
23andMers587783169
23andMe allrs587783169
SNP Nexus

SNPshotrs587783169
SNPdbers587783169
MSV3drs587783169
GWAS Ctlgrs587783169
Max Magnitude0
ClinVar
Risk rs587783169(;)
Alt rs587783169(;)
Reference rs587783169(T;T)
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.17426107delA
CLNSRC
CLNACC RCV000144992.1,