Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
rs2165241
LOXL1-AS1 ; LOXL1
0.716 0.360 15 73929861 intron variant T/C snv 0.60 15
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 9
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv 9
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 9
rs10120688
CDKN2B-AS1
0.807 0.080 9 22056500 intron variant G/A snv 0.50 7
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 7
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 7
rs2383204
CDKN2B-AS1
0.827 0.160 9 22055049 intron variant A/G;T snv 6
rs11656696
GAS7
0.882 0.040 17 10130362 intron variant C/A snv 0.36 5
rs12377632
TLR4
0.827 0.120 9 117710452 intron variant T/A;C snv 5
rs1900004
LINC02640
0.827 0.040 10 68241124 intron variant C/T snv 0.39 5
rs10063949
SLC23A1
0.882 0.080 5 139383837 intron variant T/C snv 0.48 4
rs3793342
NOS3
0.851 0.040 7 150998107 intron variant G/A snv 0.13 4
rs6445055
FNDC3B
0.925 0.040 3 172274597 intron variant G/A snv 0.24 4
rs10038177
WDR36
0.925 0.040 5 111100751 intron variant C/T snv 0.53 0.54 3
rs10451941
OPA1
0.882 0.160 3 193637313 intron variant T/A;C snv 0.42 3
rs11720822
PDIA5
0.882 0.040 3 123150194 intron variant C/T snv 8.6E-02 6.6E-02 3
rs1279683
SLC23A2
1.000 0.040 20 5002446 intron variant G/A;C snv 3
rs2156323
VAV2
0.882 0.040 9 133855699 intron variant G/A snv 9.2E-02 3