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: rs10181042
rs10181042
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