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rs193922397

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922397(A;G)
Make rs193922397(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position17442734
GeneABCC8
is asnp
is mentioned by
dbSNPrs193922397
ebirs193922397
HLIrs193922397
Exacrs193922397
Varsomers193922397
Maprs193922397
PheGenIrs193922397
hapmaprs193922397
1000 genomesrs193922397
hgdprs193922397
ensemblrs193922397
gopubmedrs193922397
geneviewrs193922397
scholarrs193922397
googlers193922397
pharmgkbrs193922397
gwascentralrs193922397
openSNPrs193922397
23andMers193922397
23andMe allrs193922397
SNP Nexus

SNPshotrs193922397
SNPdbers193922397
MSV3drs193922397
GWAS Ctlgrs193922397
Max Magnitude0
ClinVar
Risk rs193922397(G;G)
Alt rs193922397(G;G)
Reference rs193922397(A;A)
Significance Probable-Pathogenic
Disease Neonatal diabetes mellitus
Variation info
Gene ABCC8
CLNDBN Neonatal diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17464281T>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029252.1,