CLDN2, claudin 2, 9075

N. diseases: 97; N. variants: 4
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7057398
rs7057398
0.827 0.080 X 106901299 intron variant T/C snv 0.41
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
Digestive System Diseases 0.710 1.000 2 2012 2020
dbSNP: rs12008279
rs12008279
0.882 0.080 X 106917472 intron variant A/G;T snv
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs5917027
rs5917027
1.000 0.040 X 106919404 intron variant C/A;T snv
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
Digestive System Diseases 0.700 1.000 1 2012 2012