Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10272006
SP4
0.925 0.080 7 21480514 intron variant G/A snv 0.75 1
rs10314
CLDN5
1.000 0.040 22 19523195 3 prime UTR variant C/G snv 0.15 1
rs1033772
LOC107984270
1.000 0.040 10 113486173 intron variant G/A snv 0.41 1
rs1034428
GRIA3
1.000 0.040 X 123303197 intron variant A/G;T snv 1
rs1035130
IL18R1
1.000 0.040 2 102384942 synonymous variant C/T snv 0.26 0.24 1
rs1038923
GRIP1
1.000 0.040 12 66455628 intron variant T/C snv 0.66 1
rs1039621 1.000 0.040 7 158836378 intergenic variant T/C snv 0.13 1
rs10399805
CHI3L1
0.851 0.240 1 203186870 upstream gene variant G/A;T snv 6
rs10399931
CHI3L1
0.807 0.320 1 203186952 upstream gene variant T/A;C snv 6
rs1040716
PDE4B
1.000 0.040 1 66311907 intron variant A/T snv 0.37 1
rs10420331
CACNG8
1.000 0.040 19 53965814 intron variant G/A snv 0.48 1
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs1042357
ALOX12 ; ALOX12-AS1
0.925 0.040 17 7001742 synonymous variant T/C;G snv 0.59 2
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 7
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042779
ITIH1
0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 1
rs1044120
NDUFS1
1.000 0.040 2 206123849 3 prime UTR variant C/A;T snv 1
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs10447760 0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17 4
rs1045280
ARRB2
0.882 0.160 17 4719343 synonymous variant C/T snv 0.71 0.62 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10457180
FOXO3
1.000 0.040 6 108643836 intron variant G/A snv 0.52 1
rs1045881
NRXN1
1.000 0.040 2 49921834 3 prime UTR variant C/T snv 0.15 1
rs1046778
AS3MT ; BORCS7-ASMT ; LOC107984265
0.851 0.160 10 102901727 3 prime UTR variant T/C snv 0.30 3
rs10489202
MPC2
0.925 0.080 1 167933841 intron variant G/T snv 0.20 1