Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1163944538
TMEM94
0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1352010373
TMEM94
0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs61755320
SPG7
0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 41
rs28937900
FKRP
0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 37
rs151344517
LOC107985154 ; AFG3L2 ; TUBB6
0.742 0.320 18 12337505 missense variant C/T snv 31
rs1555735545
STRN4 ; FKRP
0.851 0.160 19 46746071 5 prime UTR variant G/A snv 22
rs397507478
BRAF
0.790 0.440 7 140777014 missense variant C/A snv 12
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs797045032
CLCN1
0.827 0.280 7 143321720 missense variant GG/TC mnv 11
rs121912683
SLC25A4
0.851 0.200 4 185145020 missense variant C/A snv 4.0E-06 7.0E-06 9
rs7136446
IGF1 ; LINC02456
0.882 0.160 12 102444737 intron variant C/T snv 0.66 8
rs121908216
CACNA1A
0.882 0.200 19 13235702 missense variant C/T snv 7
rs1048101
ADRA1A
0.882 0.120 8 26770511 missense variant A/G snv 0.52 0.56 5
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs5574
NPY ; LOC107986777
0.882 0.200 7 24289514 synonymous variant C/T snv 0.43 0.43 5
rs796053124
SCN2A
0.882 0.080 2 165354232 missense variant G/T snv 4
rs3743077
CHRNA3
1.000 0.040 15 78602554 intron variant C/T snv 0.31 3
rs77485247
HRH4
0.925 0.080 18 24460578 upstream gene variant T/A snv 3
rs144948296
STRC ; CKMT1B
0.925 0.120 15 43604750 stop gained G/A;C snv 1.8E-04 3
rs16979956
BMX ; ACE2
X 15525068 intron variant C/T snv 4.0E-04 2
rs35697037
BMX ; ACE2
X 15523993 intron variant G/A snv 0.37 2
rs2304297
CHRNA6
8 42753056 3 prime UTR variant G/C snv 0.39 2