Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2249296
rs2249296
CLCA2
0.925 0.040 1 86444581 intron variant T/C snv 0.85
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs2249296
rs2249296
CLCA2
0.925 0.040 1 86444581 intron variant T/C snv 0.85
CUI: C0949272
Disease: IIeocolitis
IIeocolitis 		0.700 1.000 1 2015 2015