Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs1518111 0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs4740 0.827 0.240 19 4236999 missense variant G/A snv 0.34 0.39 8
rs1313275799 1.000 0.080 15 51002561 stop gained C/T snv 4.0E-06 2
rs74315444 1.000 21 33426974 missense variant C/A snv 2