Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2756109
ABCC2
10 99798989 intron variant G/T snv 0.53 1
rs138105638
CYP3A4
7 99766440 stop gained G/A;T snv 6.4E-05 7.7E-05 3
rs80026734
CYP3A5 ; ZSCAN25
7 99676132 missense variant C/T snv 1
rs9524885
ABCC4
13 95283335 intron variant T/C snv 0.63 2
rs4584690
ABCC4
13 95027878 intron variant T/C;G snv 1
rs7335912 13 95015426 upstream gene variant A/G snv 0.16 1
rs941601
SERPINA6
14 94305204 intron variant C/T snv 0.19 1
rs885479
MC1R
0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs3212361
MC1R
16 89918814 5 prime UTR variant G/A snv 0.34 1
rs13093031 1.000 0.120 3 88809891 intergenic variant A/G snv 0.17 2
rs12633508 3 88765985 intergenic variant T/C snv 0.23 1
rs806378
CNR1
1.000 0.040 6 88149832 intron variant C/T snv 0.21 2
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894561
CSNK1D
0.882 0.120 17 82265743 missense variant T/C snv 4.0E-06 7.0E-06 5
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs1445287184
LOC105369867 ; PTPRQ
1.000 0.120 12 80670365 stop gained C/T snv 3.2E-05 2.8E-05 7
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs397514698
GNAQ
0.667 0.400 9 77797577 missense variant C/T snv 52
rs1972597 1.000 0.040 17 77598082 intron variant T/C snv 0.31 2
rs80338761
SEPTIN9
0.882 0.080 17 77402298 missense variant C/T snv 4
rs7718461
CRHBP
5 76962223 intron variant A/G snv 0.51 1