Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs7804372
CAV1
0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs28360071
XRCC4
0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs6869366
XRCC4 ; TMEM167A
0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs3807987
CAV1
0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs2285053
MMP2
0.752 0.320 16 55478465 intron variant C/T snv 0.12 15
rs28360317
XRCC4
0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs2075685
TMEM167A ; XRCC4
0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs5751129
XRCC6 ; DESI1
0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs3813867
LOC107984284 ; CYP2E1
0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs1380576
MDM4
0.763 0.240 1 204519150 intron variant G/C snv 0.57 10
rs132774
XRCC6
0.776 0.280 22 41635949 intron variant C/G snv 0.69 9
rs5743312
TLR3
0.827 0.160 4 186079102 intron variant C/T snv 0.14 9
rs9288518
XRCC5
0.776 0.240 2 216196997 intron variant A/G snv 0.35 9
rs1453414
TRIM5 ; OR52N2
0.827 0.080 11 5807854 intron variant G/C;T snv 7
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 7
rs6547741
GPN1
0.807 0.080 2 27633057 intron variant G/A snv 0.53 7
rs6553010
LOC105377596 ; MTNR1A
0.851 0.240 4 186535189 intron variant G/A snv 0.23 7
rs7664413
VEGFC ; LOC105377555
0.851 0.160 4 176687553 intron variant C/T snv 0.24 0.25 7