Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1784594
rs1784594
1 1.000 0.080 6 161961702 intron variant A/G snv 0.40 0.010 1.000 1 2013 2013
dbSNP: rs34886500
rs34886500
2 0.925 0.080 9 21971064 missense variant G/A;C snv 0.010 1.000 1 1999 1999
dbSNP: rs768477694
rs768477694
1 1.000 0.080 12 57751572 missense variant A/G snv 4.0E-06 0.010 1.000 1 1999 1999