Have questions? Visit https://www.reddit.com/r/SNPedia

rs193922406

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922406(G;G)
Make rs193922406(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17393752
GeneABCC8
is asnp
is mentioned by
dbSNPrs193922406
ebirs193922406
HLIrs193922406
Exacrs193922406
Varsomers193922406
Maprs193922406
PheGenIrs193922406
hapmaprs193922406
1000 genomesrs193922406
hgdprs193922406
ensemblrs193922406
gopubmedrs193922406
geneviewrs193922406
scholarrs193922406
googlers193922406
pharmgkbrs193922406
gwascentralrs193922406
openSNPrs193922406
23andMers193922406
23andMe allrs193922406
SNP Nexus

SNPshotrs193922406
SNPdbers193922406
MSV3drs193922406
GWAS Ctlgrs193922406
Max Magnitude0
ClinVar
Risk rs193922406(G;G)
Alt rs193922406(G;G)
Reference rs193922406(T;T)
Significance Probable-Pathogenic
Disease Neonatal diabetes mellitus
Variation info
Gene ABCC8
CLNDBN Neonatal diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17415299A>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029268.1,