Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6961071 1.000 0.120 7 156182007 downstream gene variant A/G;T snv 0.47 2
rs778056858
NTRK1
1.000 0.080 1 156866944 missense variant T/C snv 8.0E-06 7.0E-06 2
rs748653984
NTRK1
1.000 0.080 1 156868159 missense variant T/A;C snv 4.0E-06; 4.0E-06 2
rs769854785
NTRK1
1 156871656 synonymous variant C/T snv 1
rs6334
NTRK1
1.000 0.080 1 156876441 missense variant G/A;C;T snv 0.22; 4.0E-06 3
rs943552 1 156885826 downstream gene variant C/T snv 9.7E-02 2
rs179971
ATXN1
6 16362511 intron variant C/T snv 0.66 1
rs7734804
LOC105377703
5 164919530 intron variant G/T snv 8.3E-02 2
rs3872309
NBPF1
1 16564838 missense variant C/T snv 1
rs6746030
SCN1A-AS1 ; SCN9A
0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs4369876
SCN9A ; SCN1A-AS1
2 166272746 missense variant C/A snv 3.3E-02 1.3E-02 1
rs12478318
SCN1A-AS1 ; SCN9A
2 166277030 missense variant T/G snv 3.7E-02 1.3E-02 1
rs879254102
SCN9A ; SCN1A-AS1
2 166277257 missense variant C/T snv 1
rs11898284
SCN1A-AS1 ; SCN9A
2 166325017 intron variant A/G snv 0.15 1
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs3845446
CACNA1E
1 181797301 intron variant T/C snv 6.3E-02 3
rs2206593
PTGS2
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95 3
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs5277
PACERR ; PTGS2
0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 9
rs2383515 1 186683820 upstream gene variant G/A;T snv 1
rs5993882
COMT
22 19950010 intron variant T/C;G snv 2
rs740603
COMT
0.925 0.040 22 19957654 intron variant A/G snv 0.48 3
rs6269
COMT ; MIR4761
0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs6267
MIR4761 ; COMT
0.827 0.200 22 19962740 missense variant G/A;T snv 4.8E-05; 1.4E-02 9