Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs885479
MC1R
0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs1409851868
EPHA3
0.882 0.080 3 89399325 missense variant A/G snv 6
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs701848
PTEN
0.807 0.280 10 87966988 3 prime UTR variant T/C snv 0.33 10
rs2735343
PTEN
0.790 0.240 10 87945672 non coding transcript exon variant G/C snv 0.39 11
rs139832701
CAV3
0.925 0.080 3 8773124 intron variant T/G snv 0.13 3
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs1202184
ABCB1
0.851 0.120 7 87584585 intron variant C/T snv 0.39 7
rs1922242
ABCB1
0.827 0.120 7 87544351 intron variant A/T snv 0.43 8
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2349775
NXPH1
0.851 0.120 7 8678450 intron variant G/A;C snv 6
rs1187329
NTRK2
0.925 0.080 9 84674365 intron variant A/G snv 0.52 3
rs1187323
NTRK2
0.882 0.080 9 84668501 upstream gene variant C/A;G;T snv 5
rs1212171
NTRK2
0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs11636753
CHRNB4
0.882 0.120 15 78636604 intron variant G/T snv 0.35 4