rs587777167, RAB3GAP2

N. diseases: 2
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.
Martsolf syndrome
CUI: C0796037
Disease: Martsolf syndrome
3 0.925 0.240 1 220191279 missense variant G/A snv 1.6E-05 7.3E-06 0.700 1.000 2 2013 2014
WARBURG MICRO SYNDROME 2
CUI: C3280214
Disease: WARBURG MICRO SYNDROME 2
7 0.925 0.240 1 220191279 missense variant G/A snv 1.6E-05 7.3E-06 0.700 1.000 1 2013 2013