Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1013278 1.000 0.040 7 117963766 regulatory region variant G/A;C snv 1
rs10152898 1.000 0.040 15 73962780 intergenic variant G/A;T snv 1
rs190298731 1.000 0.040 6 148738155 intergenic variant A/C;T snv 1
rs2024211 1.000 0.040 7 116512971 downstream gene variant A/C snv 0.27 1
rs2935057 1.000 0.040 6 170139691 intron variant A/G;T snv 1
rs3116139 1.000 0.040 19 51375780 upstream gene variant C/A;T snv 1
rs504022 1.000 0.040 21 43311258 regulatory region variant T/G snv 0.91 1
rs56233426 1.000 0.040 3 186411027 intergenic variant A/G snv 0.50 1
rs61861119 1.000 0.040 10 93182666 intergenic variant A/G snv 0.45 1
rs8141433 1.000 0.040 22 19866483 intergenic variant A/G;T snv 1
rs7034696
ADAMTSL1
1.000 0.040 9 18804132 intron variant C/T snv 0.27 1
rs7663205
AFAP1
1.000 0.040 4 7887369 intron variant C/T snv 0.45 1
rs10505100
ANGPT1
1.000 0.040 8 107266388 intron variant C/A snv 0.13 1
rs61394862
ANKH
1.000 0.040 5 14850985 intron variant C/G;T snv 1
rs1020338837
AZI2
1.000 0.040 3 28340470 missense variant T/C;G snv 4.0E-06 1
rs566095092
AZI2
1.000 0.040 3 28336841 missense variant T/C snv 4.0E-06 2.1E-05 1
rs548246291
B3GALT6 ; SDF4
1.000 0.040 1 1232945 missense variant G/A snv 4.0E-05 2.8E-05 1
rs1401907822
B4GALT7
1.000 0.040 5 177608566 missense variant G/A snv 1
rs9284802
CADM2
1.000 0.040 3 85046615 intron variant G/A snv 0.44 1
rs540694424
CNTNAP2
1.000 0.040 7 146650935 intron variant G/C;T snv 1
rs774766411
CXCL8
1.000 0.040 4 73741625 missense variant A/G snv 1.2E-05 1
rs369115487
CYP1B1-AS1 ; CYP1B1
1.000 0.040 2 38075373 missense variant T/C snv 1.6E-05 1.4E-05 1
rs757691206
CYP1B1 ; CYP1B1-AS1
1.000 0.040 2 38074662 missense variant C/A;G snv 4.0E-06; 4.0E-06 1
rs151326733
DERA
1.000 0.040 12 16036544 intron variant G/C snv 1.0E-02 1
rs542340
DNAJC24
1.000 0.040 11 31387891 intron variant A/G;T snv 5.5E-03 1