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rs193922408

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922408(A;A)
Make rs193922408(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position17393122
GeneABCC8
is asnp
is mentioned by
dbSNPrs193922408
ebirs193922408
HLIrs193922408
Exacrs193922408
Varsomers193922408
Maprs193922408
PheGenIrs193922408
hapmaprs193922408
1000 genomesrs193922408
hgdprs193922408
ensemblrs193922408
gopubmedrs193922408
geneviewrs193922408
scholarrs193922408
googlers193922408
pharmgkbrs193922408
gwascentralrs193922408
openSNPrs193922408
23andMers193922408
23andMe allrs193922408
SNP Nexus

SNPshotrs193922408
SNPdbers193922408
MSV3drs193922408
GWAS Ctlgrs193922408
Max Magnitude0
ClinVar
Risk rs193922408(A;A)
Alt rs193922408(A;A)
Reference rs193922408(G;G)
Significance Probable-Pathogenic
Disease Neonatal diabetes mellitus
Variation info
Gene ABCC8
CLNDBN Neonatal diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17414669C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029270.1,