Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12948783
RHBDF2
17 76503318 upstream gene variant G/A;C;T snv 1
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs11988795
TRPA1 ; MSC-AS1
8 72037366 intron variant C/G;T snv 1
rs200192163
MSC-AS1 ; TRPA1
8 72036453 missense variant C/A;G snv 1.6E-05 1
rs1057518946
GJB1
0.882 0.080 X 71223816 missense variant G/T snv 8
rs765502022
UGT2B7
0.827 0.240 4 69112695 missense variant T/C snv 1.6E-05 8
rs773030005
UGT2B7
1.000 0.040 4 69107204 synonymous variant A/C;G snv 4.0E-06; 6.8E-05 2
rs7439366
UGT2B7
0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs749415280
UGT2B7
1.000 0.120 4 69096638 missense variant A/G snv 2
rs4587017
UGT2B7
4 69081680 intron variant T/G snv 0.63 1
rs2069705
IFNG-AS1 ; IFNG
0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 17
rs121908552
SCN4A ; LOC105371858
0.763 0.160 17 63964587 missense variant C/A;G;T snv 4.0E-06 14
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs80338958
SCN4A
0.790 0.200 17 63945614 missense variant C/A;T snv 1.6E-05; 5.6E-05 9
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
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs74315431
VAPB
0.732 0.080 20 58418318 missense variant C/T snv 4.0E-06 15
rs2653349
HCRTR2
0.882 0.120 6 55277539 missense variant A/G;T snv 0.84; 4.0E-06 5
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 6
rs10483639 1.000 0.040 14 54839739 downstream gene variant G/C snv 0.26 3
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1051660
OPRK1
1.000 0.080 8 53251002 synonymous variant C/A;T snv 0.11 3