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rs193922396

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922396(C;C)
Make rs193922396(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17442744
GeneABCC8
is asnp
is mentioned by
dbSNPrs193922396
ebirs193922396
HLIrs193922396
Exacrs193922396
Varsomers193922396
Maprs193922396
PheGenIrs193922396
hapmaprs193922396
1000 genomesrs193922396
hgdprs193922396
ensemblrs193922396
gopubmedrs193922396
geneviewrs193922396
scholarrs193922396
googlers193922396
pharmgkbrs193922396
gwascentralrs193922396
openSNPrs193922396
23andMers193922396
23andMe allrs193922396
SNP Nexus

SNPshotrs193922396
SNPdbers193922396
MSV3drs193922396
GWAS Ctlgrs193922396
Max Magnitude0
ClinVar
Risk rs193922396(C;C)
Alt rs193922396(C;C)
Reference rs193922396(T;T)
Significance Probable-Pathogenic
Disease Neonatal diabetes mellitus
Variation info
Gene ABCC8
CLNDBN Neonatal diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17464291A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029251.1,