Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs4539
CYP11B2 ; GML
0.925 0.080 8 142915123 missense variant T/C snv 0.42 0.38 4
rs6471
CYP21A2
0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 24
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs2234922
EPHX1
0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs536562413
FBXO11 ; MSH6
0.732 0.240 2 47799934 missense variant A/G snv 1.2E-05 7.0E-06 15
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs763539313
GAPDH
12 6537702 missense variant A/G snv 2.0E-05 4.9E-05 1
rs61734277
GCM2
0.882 0.080 6 10874672 missense variant A/C snv 9.1E-03 8.6E-03 5
rs142287570
GCM2
1.000 6 10874335 missense variant T/G snv 6.6E-04 4.9E-04 2
rs371918069
GCM2
1.000 6 10874372 missense variant C/T snv 5.6E-05 5.6E-05 2
rs142163070
GML ; CYP11B1
8 142877100 missense variant T/C snv 2.0E-04 4.5E-04 1
rs1290398674
GNAS
0.851 0.240 20 58854075 missense variant G/A;T snv 5
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs770460061
GSTP1
0.742 0.240 11 67585239 missense variant T/C;G snv 4.0E-06; 1.2E-05 14
rs146462069
IGSF1
X 131278706 missense variant T/C;G snv 3.8E-05; 9.5E-03 2
rs2855798
KCNJ1 ; LOC107984409
11 128863066 intron variant G/T snv 0.21 1
rs386352319
KCNJ5
0.827 0.080 11 128911724 missense variant G/A;C snv 8
rs386352318
KCNJ5
0.925 0.080 11 128911776 missense variant T/G snv 4
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63