Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10166942
TRPM8
0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40 4
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1044397
CHRNA4
0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 7
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10483639 1.000 0.040 14 54839739 downstream gene variant G/C snv 0.26 3
rs104894379
TBX5
1.000 0.120 12 114398675 stop gained G/A;C;T snv 2
rs104894561
CSNK1D
0.882 0.120 17 82265743 missense variant T/C snv 4.0E-06 7.0E-06 5
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1050565
BLMH
1.000 0.080 17 30249058 missense variant T/C snv 0.30 0.29 2
rs1051660
OPRK1
1.000 0.080 8 53251002 synonymous variant C/A;T snv 0.11 3
rs1057518927
OAT
0.925 0.080 10 124402952 missense variant T/C snv 4
rs1057518946
GJB1
0.882 0.080 X 71223816 missense variant G/T snv 8
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11466112
NGF-AS1 ; NGF
1.000 0.080 1 115286135 missense variant G/A snv 1.6E-05 7.0E-06 3
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs11709492
SCN11A
3 38904493 intron variant C/T snv 0.26 1
rs11720013
SCN11A
3 38924745 intron variant G/T snv 1.0E-01 1
rs11720988
SCN11A
3 38865054 intron variant G/A snv 0.26 1
rs1172682117
ERG
21 38403690 synonymous variant T/G snv 4.0E-06 1
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs11898284
SCN1A-AS1 ; SCN9A
2 166325017 intron variant A/G snv 0.15 1