Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7461115 1.000 0.040 8 20014029 intergenic variant C/A;G snv 0.37 4
rs7575840 1.000 0.040 2 21050618 intergenic variant G/T snv 0.26 4
rs768925824
LDLR
0.925 0.040 19 11110693 missense variant G/A snv 4.0E-06 4
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs10838681
NR1H3
1.000 0.040 11 47253513 intron variant G/A snv 0.34 3
rs11600380 1.000 0.040 11 116799466 intergenic variant T/C snv 6.6E-02 3
rs12988520
UGT1A6 ; UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7
1.000 0.040 2 233698748 intron variant A/C snv 0.51 3
rs13226650
MLXIPL
1.000 0.040 7 73602675 intron variant A/G snv 0.19 3
rs1502593
SCD
1.000 0.040 10 100349445 intron variant G/A snv 0.34 3
rs1797912
PPARG
1.000 0.040 3 12428740 intron variant A/C snv 0.33 3
rs2361502
MROH2A
1.000 0.040 2 233790144 intron variant T/C snv 0.30 3
rs2454727
HCAR2
0.925 0.040 12 122702333 missense variant C/T snv 3
rs2845573
FADS2
1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 3
rs3093068 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 3
rs7314976
HCAR2
0.925 0.040 12 122702353 missense variant G/A;C snv 3.9E-02; 4.5E-06 3
rs7841189 1.000 0.040 8 19987865 TF binding site variant C/T snv 0.15 3
rs10484092
FRMD6-AS2 ; FRMD6
1.000 0.040 14 51489516 intron variant A/G snv 4.8E-02 2
rs10488698
BUD13
1.000 0.040 11 116763231 missense variant G/A snv 6.4E-02 4.8E-02 2
rs11099680
NR3C2
1.000 0.040 4 148182095 intron variant G/A snv 0.78 2
rs11774572 1.000 0.040 8 11589291 regulatory region variant C/G;T snv 2
rs12503643
ACSL1 ; LOC105377587
1.000 0.040 4 184824934 intron variant G/A;T snv 2
rs13189262 1.000 0.040 5 57978493 intergenic variant G/T snv 0.16 2
rs1558162
POU6F2 ; LOC105375238
1.000 0.040 7 39471024 intron variant C/G;T snv 2
rs16885704 1.000 0.040 6 74829426 regulatory region variant A/G snv 6.1E-02 2
rs16940170
ALDH1A2
1.000 0.040 15 58392083 intron variant G/A snv 0.15 2