Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs118203347
TSC1
1.000 0.120 9 132927208 missense variant T/C snv 7.0E-06 1
rs118203385
TSC1
1.000 0.120 9 132923383 missense variant A/C;G snv 1
rs1323541164
TSC1
1.000 0.120 9 132921834 missense variant A/C snv 1
rs11892031
UGT1A10 ; UGT1A8
0.882 0.120 2 233656637 intron variant A/C;T snv 5
rs779682021
CYP1A1
0.882 0.120 15 74721227 missense variant A/C snv 5
rs887569
EZH2
0.882 0.120 7 148808210 intron variant C/T snv 0.73 5
rs10743980
LRP6
0.882 0.120 12 12259861 intron variant T/A;C;G snv 4
rs2073859
LIMK2
0.882 0.120 22 31278567 3 prime UTR variant G/A snv 4.0E-02 4
rs1014971 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 3
rs10234749 0.882 0.120 7 152690784 regulatory region variant T/C;G snv 3
rs10775480
LOC105372093 ; SLC14A1
0.882 0.120 18 45737317 intron variant T/C snv 0.61 3
rs11077654
SLC39A11
0.882 0.120 17 73010373 intron variant A/C snv 0.69 3
rs11191438
AS3MT ; BORCS7-ASMT
0.882 0.120 10 102878107 intron variant G/A;C snv 3
rs1135612
POR
0.882 0.120 7 75980359 synonymous variant A/G;T snv 0.28 3
rs11543198
CLK3
0.882 0.120 15 74619987 missense variant G/A;T snv 0.11 3
rs11871756
SLC39A11
0.882 0.120 17 72730105 intron variant C/G snv 0.11 3
rs1189516787
CEBPA ; CEBPA-DT
0.882 0.120 19 33301681 missense variant C/G snv 7.1E-06 3
rs1203030830
EGFR
0.882 0.120 7 55155873 synonymous variant T/C snv 4.0E-06 3
rs1336331763
SULT1A1
0.882 0.120 16 28606796 missense variant G/A snv 4.0E-06 3
rs140241283
MTHFR
0.882 0.120 1 11796249 start lost A/G;T snv 4.0E-06; 4.0E-06 3
rs1428779969
PXN
0.882 0.120 12 120223776 missense variant G/A snv 7.0E-06 3
rs1484761909
GSTM1 ; GSTM2
0.882 0.120 1 109688224 missense variant A/G snv 3.0E-05 3.8E-05 3
rs17674580
SLC14A1 ; LOC105372093
0.882 0.120 18 45729946 5 prime UTR variant C/A;T snv 3
rs197414
DDX20
0.882 0.120 1 111766501 missense variant C/A;T snv 0.12; 4.0E-06 3
rs2042329
CWC27
0.882 0.120 5 64771925 intron variant T/C;G snv 3