Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11088680 0.925 0.080 21 13514758 upstream gene variant A/G snv 0.30 2
rs1887427 0.925 0.080 9 4979730 upstream gene variant A/G snv 0.21 2
rs1892901 0.925 0.080 11 65903422 upstream gene variant G/A snv 9.5E-03 2
rs26160 0.925 0.080 5 145353893 intron variant T/C snv 4.5E-03 2
rs36012910 0.925 0.080 2 25345310 upstream gene variant A/C;G snv 2
rs4145643 0.925 0.080 10 60803097 regulatory region variant G/C;T snv 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1305398818
ABCG2
0.925 0.080 4 88131886 missense variant G/A;C snv 4.0E-06; 4.0E-06 4
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs6713088
ACYP2
0.763 0.200 2 54118332 intron variant C/G snv 0.48 9
rs11896604
ACYP2
0.776 0.200 2 54252062 intron variant C/A;G;T snv 8
rs843706
ACYP2 ; TSPYL6
0.807 0.160 2 54253232 3 prime UTR variant C/A snv 0.42 6
rs4963
ADD1
0.827 0.120 4 2915035 missense variant C/G;T snv 0.20 0.18 6
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs17033
ADH1B
0.925 0.080 4 99307788 3 prime UTR variant T/C snv 9.6E-02 3
rs283411
ADH1C ; ADH1B
0.925 0.080 4 99344800 intron variant C/A;T snv 2
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs822395
ADIPOQ
0.776 0.240 3 186849018 intron variant C/A;G snv 10
rs12733285
ADIPOR1
0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs1342387
ADIPOR1
0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs184003
AGER
0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134