Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1555206402
HMBS
0.790 0.320 11 119093274 stop lost GCCCATTAACTGGTTTGTGGGGCACAGATGCCTGGGTTGCTGCTGTCCAGTGCCT/- delins 26
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1555640521
LAMA1
0.790 0.320 18 6942110 frameshift variant A/- delins 15
rs886037774
LPL
0.882 0.120 8 19955993 missense variant T/C snv 7
rs886037775
LPL
0.882 0.120 8 19960948 missense variant A/T snv 7
rs349358
KCNB2
8 72539240 intron variant C/T snv 0.88 3
rs763004980
ACAD9
3 128906139 missense variant G/A snv 1.2E-05 1.4E-05 2
rs150283105
ACAD9 ; KIAA1257
3 128909410 missense variant C/T snv 7.2E-05 1.3E-04 2
rs6806362 3 103172459 intergenic variant G/T snv 1.7E-02 1
rs6807670
HTR3C
3 184060510 3 prime UTR variant G/A snv 0.61 1