Source: GWASDB

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: rs10188217
rs10188217
PUS10
0.925 0.080 2 60990407 intron variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2008 2011
dbSNP: rs13003464
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2008 2012
dbSNP: rs10181042
rs10181042
PUS10
1.000 0.040 2 60997124 intron variant C/T snv 0.41
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2010