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rs193922355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922355(C;G)
Make rs193922355(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position27924291
GenePDX1
is asnp
is mentioned by
dbSNPrs193922355
ebirs193922355
HLIrs193922355
Exacrs193922355
Varsomers193922355
Maprs193922355
PheGenIrs193922355
hapmaprs193922355
1000 genomesrs193922355
hgdprs193922355
ensemblrs193922355
gopubmedrs193922355
geneviewrs193922355
scholarrs193922355
googlers193922355
pharmgkbrs193922355
gwascentralrs193922355
openSNPrs193922355
23andMers193922355
23andMe allrs193922355
SNP Nexus

SNPshotrs193922355
SNPdbers193922355
MSV3drs193922355
GWAS Ctlgrs193922355
Max Magnitude0
ClinVar
Risk rs193922355(G;G)
Alt rs193922355(G;G)
Reference rs193922355(C;C)
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.28498428C>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030079.1,