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rs193922565

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922565(C;C)
Make rs193922565(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17388087
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs193922565
ebirs193922565
HLIrs193922565
Exacrs193922565
Varsomers193922565
Maprs193922565
PheGenIrs193922565
hapmaprs193922565
1000 genomesrs193922565
hgdprs193922565
ensemblrs193922565
gopubmedrs193922565
geneviewrs193922565
scholarrs193922565
googlers193922565
pharmgkbrs193922565
gwascentralrs193922565
openSNPrs193922565
23andMers193922565
23andMe allrs193922565
SNP Nexus

SNPshotrs193922565
SNPdbers193922565
MSV3drs193922565
GWAS Ctlgrs193922565
Max Magnitude0
ClinVar
Risk rs193922565(C;C)
Alt rs193922565(C;C)
Reference rs193922565(T;T)
Significance Probable-Pathogenic
Disease Neonatal diabetes mellitus
Variation info
Gene KCNJ11
CLNDBN Neonatal diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17409634A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030105.1,