Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs4818
COMT ; MIR4761
0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs165774
COMT
0.807 0.120 22 19965038 3 prime UTR variant G/A snv 0.27 11
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs6269
COMT ; MIR4761
0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs9332377
ARVCF ; COMT
0.882 0.120 22 19968169 intron variant C/A;T snv 5
rs165656
COMT
0.925 0.200 22 19961340 intron variant G/A;C;T snv 5
rs2273206
ESR1
0.851 0.280 6 152061176 intron variant G/T snv 0.17 0.22 5
rs758537709
TTN-AS1 ; TTN
0.882 0.200 2 178549459 missense variant G/A snv 4.1E-05 7.7E-05 4
rs281864931
TTN ; TTN-AS1
0.882 0.200 2 178527151 missense variant T/G snv 4
rs858339
ENPP1
1.000 0.120 6 131832757 intron variant T/A snv 0.30 3
rs1676303 14 76525821 intron variant C/T snv 0.79 2
rs5993882
COMT
22 19950010 intron variant T/C;G snv 2
rs13078961 3 137968843 intergenic variant G/C snv 7.6E-02 1
rs60249166 13 31510764 intergenic variant C/T snv 0.15 1
rs73271865 7 21359709 intergenic variant C/T snv 5.7E-02 1
rs1531554
BAHCC1
17 81406747 intron variant T/C snv 0.51 1
rs73460075
DMD
X 32265375 intron variant G/C snv 5.0E-02 1
rs6574293
ESRRB
14 76404257 intron variant A/G snv 0.89 1
rs2241719
TGFB1 ; CCDC97
19 41323676 3 prime UTR variant T/A;C snv 1