rs387906777, PDX1

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
DIABETES MELLITUS, PERMANENT NEONATAL
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
108 0.851 0.120 13 27924382 missense variant A/G snv 0.700 1.000 2 2003 2010
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE IV (disorder)
CUI: C1833382
Disease: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE IV (disorder)
6 0.851 0.120 13 27924382 missense variant A/G snv 0.700 0
PANCREATIC AGENESIS 1
CUI: C3891828
Disease: PANCREATIC AGENESIS 1
5 0.851 0.120 13 27924382 missense variant A/G snv 0.700 0
Exocrine pancreatic insufficiency
CUI: C0267963
Disease: Exocrine pancreatic insufficiency
26 0.851 0.120 13 27924382 missense variant A/G snv 0.010 1 2010 2010