Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10744826
UBE3B
12 109527707 intron variant C/G snv 0.57 3
rs4841465
XKR6
8 10962344 intron variant C/G;T snv 3
rs11102001
GSTM5 ; EPS8L3
0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 4
rs4260308 20 10981537 intron variant G/A snv 0.41 2
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs143020224
SMARCA4
19 11076648 intron variant C/G;T snv 2
rs10849915
CCDC63
0.925 0.080 12 110895818 intron variant T/C snv 0.39 3
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 4
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs4767293 12 112025492 downstream gene variant A/G snv 0.53 3
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs7096937
GPAM
10 112190660 intron variant T/C snv 0.72 5
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71 5
rs10741534 11 11233360 intergenic variant T/A;C snv 2
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27