Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs1805094 0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16