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: rs6784820
rs6784820
RHOA ; TCTA
1.000 0.040 3 49413431 intron variant A/G snv 0.40
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2008 2008
dbSNP: rs7648841
rs7648841
RHOA
1.000 0.040 3 49379392 intron variant G/A snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2007 2007