Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs4636297
EGFL7 ; MIR126
0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 13
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs2241767
ADIPOQ-AS1 ; ADIPOQ
0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs4612666
NLRP3
0.763 0.440 1 247435768 intron variant T/C snv 0.65 10
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs4962153
ADAMTS13 ; CACFD1
0.925 0.120 9 133458632 intron variant A/G snv 0.79 9
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs927650
CYP24A1
0.763 0.240 20 54156202 intron variant T/A;C snv 9
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs11896604
ACYP2
0.776 0.200 2 54252062 intron variant C/A;G;T snv 8