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rs570388861

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs570388861(A;A)
Make rs570388861(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17408415
GeneABCC8
is asnp
is mentioned by
dbSNPrs570388861
ebirs570388861
HLIrs570388861
Exacrs570388861
Varsomers570388861
Maprs570388861
PheGenIrs570388861
hapmaprs570388861
1000 genomesrs570388861
hgdprs570388861
ensemblrs570388861
gopubmedrs570388861
geneviewrs570388861
scholarrs570388861
googlers570388861
pharmgkbrs570388861
gwascentralrs570388861
openSNPrs570388861
23andMers570388861
23andMe allrs570388861
SNP Nexus

SNPshotrs570388861
SNPdbers570388861
MSV3drs570388861
GWAS Ctlgrs570388861
Max Magnitude0
ClinVar
Risk rs570388861(A,C;A,C)
Alt rs570388861(A,C;A,C)
Reference rs570388861(G;G)
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.17429962G>A
CLNSRC Counsyl
CLNACC RCV000169216.1, RCV000201910.1,