Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1941404
NNMT
0.882 0.120 11 114298316 non coding transcript exon variant A/G snv 0.59 3
rs198388
NPPB
0.851 0.160 1 11857283 downstream gene variant C/G;T snv 4
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs200960801
ESR1
0.827 0.200 6 151944488 missense variant A/G snv 4.0E-06 6
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv 7
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs2222823
MYLK
0.925 0.080 3 123885940 upstream gene variant T/A snv 0.14 4
rs2228314
SREBF2
0.790 0.360 22 41880738 missense variant G/C snv 0.34 0.38 8
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs2302685
BCL2L14 ; LRP6
0.827 0.240 12 12148964 missense variant C/T snv 0.85 0.84 5
rs2306283
SLCO1B1
0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs2523608
MIR6891 ; HLA-B
0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19 6
rs267606661
APOE
0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs2811712
CDKN2B-AS1
0.882 0.080 9 21998036 intron variant G/A snv 0.85 5