Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs4636297
EGFL7 ; MIR126
0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5
rs974453
SLCO1C1
1.000 0.080 12 20737008 intron variant A/G;T snv 3
rs12090554
LOC107985239 ; LINC01350
0.925 0.080 1 185583216 intron variant G/A snv 0.15 2
rs13290387
PAPPA
0.925 0.120 9 116227647 intron variant G/C snv 0.54 2
rs1353342
PCSK5
0.925 0.080 9 76259853 intron variant A/C snv 0.79 2
rs2227721
VTN ; SARM1
0.925 0.080 17 28370430 intron variant C/A;T snv 0.12 2
rs1140713
MIR126 ; EGFL7
1.000 0.080 9 136670833 intron variant C/T snv 0.13 1
rs1445501474
GATA6-AS1 ; GATA6
1.000 0.080 18 22168521 intron variant G/T snv 1.4E-05 1
rs2824292 0.925 0.080 21 17414857 regulatory region variant G/A snv 0.47 3
rs72653706
ABCC6
0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs1237080661
SCN5A
0.925 0.080 3 38604780 stop gained A/G;T snv 2.8E-05 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157