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rs193922399

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922399(G;G)
Make rs193922399(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17404527
GeneABCC8
is asnp
is mentioned by
dbSNPrs193922399
ebirs193922399
HLIrs193922399
Exacrs193922399
Varsomers193922399
Maprs193922399
PheGenIrs193922399
hapmaprs193922399
1000 genomesrs193922399
hgdprs193922399
ensemblrs193922399
gopubmedrs193922399
geneviewrs193922399
scholarrs193922399
googlers193922399
pharmgkbrs193922399
gwascentralrs193922399
openSNPrs193922399
23andMers193922399
23andMe allrs193922399
SNP Nexus

SNPshotrs193922399
SNPdbers193922399
MSV3drs193922399
GWAS Ctlgrs193922399
Max Magnitude0
ClinVar
Risk rs193922399(G;G)
Alt rs193922399(G;G)
Reference rs193922399(T;T)
Significance Probable-Pathogenic
Disease Neonatal diabetes mellitus
Variation info
Gene ABCC8
CLNDBN Neonatal diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17426074A>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029256.1,