rs1064795559, MORC2

N. diseases: 29
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Prominent ear helix
CUI: C4024165
Disease: Prominent ear helix
3 0.752 0.320 22 30946373 missense variant G/A snv 0.700 0
Soft, doughy skin
CUI: C1849043
Disease: Soft, doughy skin
4 0.752 0.320 22 30946373 missense variant G/A snv 0.700 0
Tremor of hands
CUI: C0239842
Disease: Tremor of hands
7 0.752 0.320 22 30946373 missense variant G/A snv 0.700 0
Unable to concentrate
CUI: C0235198
Disease: Unable to concentrate
1 0.752 0.320 22 30946373 missense variant G/A snv 0.700 0