Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 8
rs174567
FADS1 ; FADS2
1.000 0.080 11 61825533 intron variant A/G;T snv 4
rs708686
FUT6
19 5840608 upstream gene variant C/T snv 0.46 3
rs2290846
LRBA
1.000 0.040 4 150277928 missense variant G/A snv 0.20 0.18 3
rs56398830
SLC10A2
0.925 0.040 13 103049340 missense variant G/A;T snv 1.0E-02 3
rs12882491
TRAF3
0.925 0.160 14 102816936 intron variant C/T snv 0.51 3
rs686030
TTC39B
9 15304784 intron variant C/A snv 0.88 3
rs12968116
ATP8B1 ; LOC100505549
18 57655270 missense variant C/T snv 8.2E-02 8.0E-02 2
rs2292553
PNKD ; TMBIM1 ; MIR6513
2 218282080 missense variant G/A snv 0.55 0.43 2
rs2547231
SULT2A1
19 47881800 intron variant C/A snv 0.86 2
rs11641445 16 11545628 downstream gene variant C/T snv 0.36 1
rs13280055 8 11664844 intergenic variant G/A snv 8.6E-02 1
rs2469991 8 119335236 intergenic variant A/T snv 0.42 1
rs34851490 19 45881296 downstream gene variant A/G snv 0.11 1
rs6471717 8 58464798 intergenic variant G/A snv 0.70 1
rs4148808
ABCB4
7 87476479 intron variant T/C snv 0.19 1
rs17240268
ANPEP
15 89804583 missense variant G/A snv 6.9E-02 9.2E-02 1
rs17138478
HNF1B ; LOC105371754
17 37713312 intron variant C/A;T snv 0.11 1