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
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
rs6464268 0.882 0.120 7 152684065 intergenic variant A/G snv 0.23 3
rs715021 0.882 0.120 2 221196620 intergenic variant C/G snv 0.26 3
rs8102137 0.882 0.120 19 29805946 regulatory region variant T/C snv 0.24 3
rs921142 0.882 0.120 8 41311757 upstream gene variant T/C snv 0.31 3
rs4986826
AHR
0.882 0.120 7 17339533 missense variant G/A snv 7.8E-03 2.2E-02 3
rs8041357
ARID3B
0.882 0.120 15 74577097 intron variant T/C snv 6.6E-02 3
rs11191438
AS3MT ; BORCS7-ASMT
0.882 0.120 10 102878107 intron variant G/A;C snv 3
rs7257330
CCNE1
0.882 0.120 19 29810916 upstream gene variant G/A snv 0.30 3
rs1189516787
CEBPA ; CEBPA-DT
0.882 0.120 19 33301681 missense variant C/G snv 7.1E-06 3
rs8444
CERS2
0.882 0.120 1 150966095 3 prime UTR variant G/A snv 0.35 3
rs11543198
CLK3
0.882 0.120 15 74619987 missense variant G/A;T snv 0.11 3
rs2042329
CWC27
0.882 0.120 5 64771925 intron variant T/C;G snv 3
rs197414
DDX20
0.882 0.120 1 111766501 missense variant C/A;T snv 0.12; 4.0E-06 3
rs1203030830
EGFR
0.882 0.120 7 55155873 synonymous variant T/C snv 4.0E-06 3
rs771866347
GPX1
0.882 0.120 3 49358109 missense variant G/A snv 4.1E-06 3
rs9624880
GRK3
0.882 0.120 22 25588025 intron variant C/T snv 3
rs1484761909
GSTM1 ; GSTM2
0.882 0.120 1 109688224 missense variant A/G snv 3.0E-05 3.8E-05 3
rs758057623
GSTP1
0.882 0.120 11 67584520 missense variant G/A snv 3
rs10775480
LOC105372093 ; SLC14A1
0.882 0.120 18 45737317 intron variant T/C snv 0.61 3
rs140241283
MTHFR
0.882 0.120 1 11796249 start lost A/G;T snv 4.0E-06; 4.0E-06 3