Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3751143
P2RX7 ; LOC105370032
0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs4147929
ABCA7
0.882 0.120 19 1063444 intron variant A/C;G snv 3
rs1144507
ZNF202
0.925 0.080 11 123729767 missense variant A/C;G;T snv 0.68 2
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs4359426
CCL22
0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs147377392
THBD
0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs872129 0.925 0.080 1 203200263 intergenic variant A/G snv 0.19 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs884164
PLIN4
0.925 0.040 19 4521613 upstream gene variant A/G;T snv 2
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32