Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7638459
TRPC1
1.000 0.120 3 142771309 intron variant T/C snv 0.35 1
rs7639705
MCF2L2
1.000 0.120 3 183309754 missense variant T/G snv 0.26 0.27 1
rs770917264
MOK
1.000 0.120 14 102229547 stop gained G/A;C snv 4.0E-06; 1.6E-05 1
rs838136
FUT1
1.000 0.120 19 48753131 intron variant T/C snv 0.41 1
rs953239
TRPC1
1.000 0.120 3 142727363 intron variant A/C snv 0.46 1
rs9533481
ENOX1
1.000 0.120 13 43415049 intron variant T/C snv 0.78 1
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 9
rs3752462
MYH9
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs1137933
NOS2
0.882 0.160 17 27778906 synonymous variant G/A snv 0.20 0.21 4
rs2779248
NOS2
0.882 0.160 17 27800806 intron variant T/C snv 0.39 4
rs56094641
FTO
0.925 0.160 16 53772541 intron variant A/G;T snv 4
rs75444904
HPR ; TXNL4B
0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 4
rs7588550
ERBB4
0.851 0.160 2 212304043 intron variant G/A snv 0.96 4
rs117897666
LOC105370892
0.882 0.160 15 73811619 intergenic variant C/T snv 3
rs136161
APOL1
0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs1411766
LOC101927627
0.882 0.160 13 109599813 intron variant G/A;T snv 3
rs2281999
UNC13B
0.925 0.160 9 35381507 intron variant C/T snv 0.35 0.38 3
rs55703767
MFF-DT ; COL4A3
0.925 0.160 2 227256385 missense variant G/A;T snv 4.0E-06; 0.17 3
rs6997279
SLC30A8
0.882 0.160 8 116961613 intron variant G/T snv 0.20 3
rs73206603
LOC107984625
0.882 0.160 13 59495931 regulatory region variant G/C snv 4.2E-02 3
rs741301
ELMO1
0.925 0.160 7 36878390 intron variant C/T snv 0.59 3
rs10255208 0.925 0.160 7 36819038 non coding transcript exon variant A/G snv 0.46 2
rs10823108
SIRT1
0.925 0.160 10 67900736 intron variant G/A snv 7.1E-02 2
rs1531343
RPSAP52
0.925 0.160 12 65781114 intron variant G/C;T snv 2