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rs193922356

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922356(A;C)
Make rs193922356(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position27924420
GenePDX1
is asnp
is mentioned by
dbSNPrs193922356
ebirs193922356
HLIrs193922356
Exacrs193922356
Varsomers193922356
Maprs193922356
PheGenIrs193922356
hapmaprs193922356
1000 genomesrs193922356
hgdprs193922356
ensemblrs193922356
gopubmedrs193922356
geneviewrs193922356
scholarrs193922356
googlers193922356
pharmgkbrs193922356
gwascentralrs193922356
openSNPrs193922356
23andMers193922356
23andMe allrs193922356
SNP Nexus

SNPshotrs193922356
SNPdbers193922356
MSV3drs193922356
GWAS Ctlgrs193922356
Max Magnitude0
ClinVar
Risk rs193922356(C;C)
Alt rs193922356(C;C)
Reference rs193922356(A;A)
Significance Probable-Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene PDX1
CLNDBN Maturity-onset diabetes of the young, type 4
Reversed 0
HGVS NC_000013.10:g.28498557A>C
CLNSRC ClinVar LabCorp
CLNACC RCV000030081.1,