Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs4917
AHSG
0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68 9
rs4918
AHSG
0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1049636
FGG
1.000 0.080 4 154604818 3 prime UTR variant G/A snv 0.67 0.70 1
rs7172
PSMB4
1.000 0.080 1 151399662 synonymous variant G/A;C snv 0.67 1
rs2236052
RGS12
1.000 0.080 4 3316686 synonymous variant A/G snv 0.64 0.70 1
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs12632110
SEMA3F
1.000 0.080 3 50186792 intron variant A/G snv 0.63 0.62 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1801058
GRK4
0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 4
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs5888
SCARB1
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs10965215
CDKN2B-AS1
0.882 0.120 9 22029446 missense variant G/A snv 0.55 0.46 4
rs12487736
SCAP
1.000 0.080 3 47418189 missense variant C/T snv 0.54 0.47 2
rs4363
ACE
1.000 0.080 17 63497131 splice region variant G/A;C snv 0.52 2
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs6687605
LDLRAP1
1.000 0.080 1 25563141 missense variant T/A;C;G snv 1.6E-05; 0.51; 4.0E-06 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16