Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 15
rs2165241
LOXL1-AS1 ; LOXL1
0.716 0.360 15 73929861 intron variant T/C snv 0.60 15
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 9
rs10120688
CDKN2B-AS1
0.807 0.080 9 22056500 intron variant G/A snv 0.50 7
rs11024102
PLEKHA7
0.851 0.040 11 16987058 intron variant T/C snv 0.20 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
rs1015213 0.851 0.040 8 51974981 intron variant C/T snv 0.14 6
rs3918249
MMP9
0.807 0.200 20 46009497 intron variant T/C snv 0.41 6
rs518394
CDKN2B-AS1
0.827 0.160 9 22019674 intron variant G/C snv 0.30 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
rs4886782
LOXL1
1.000 0.040 15 73936469 intron variant G/A snv 0.27 5
rs10965219
CDKN2B-AS1
0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs2093210
C14orf39
1.000 0.040 14 60490561 intron variant C/T snv 0.45 4
rs3788317
TXNRD2
0.851 0.040 22 19902302 intron variant G/T snv 0.30 4
rs4337252
LOXL1
1.000 0.040 15 73934424 intron variant G/C snv 0.52 4
rs7518099
TMCO1-AS1 ; TMCO1
0.925 0.040 1 165767643 intron variant C/T snv 0.89 4
rs7555523
TMCO1
0.925 0.040 1 165749742 intron variant C/A snv 0.88 4
rs7859156
LMX1B
0.851 0.040 9 126637749 intron variant T/C snv 0.74 4
rs944801
CDKN2B-AS1
0.882 0.120 9 22051671 intron variant G/A;C snv 4