Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs1056827
CYP1B1 ; CYP1B1-AS1
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs1057519912
MED12
0.776 0.200 X 71129408 missense variant C/G;T snv 11
rs1057519966
LOC107984999 ; SPOP
0.882 0.080 17 49619064 missense variant A/C;T snv 3
rs1057519972
SPOP ; LOC107984999
0.882 0.080 17 49619327 missense variant A/T snv 3
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 14
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1058205
KLK3
0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 3
rs1058587
GDF15
0.882 0.200 19 18388612 missense variant C/G;T snv 0.24; 9.1E-06 4
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1060501201
TP53
0.925 0.080 17 7674190 missense variant T/C;G snv 4
rs10740051
NCOA4
0.925 0.080 10 46025670 intron variant C/T snv 0.24 2
rs10749408 0.925 0.080 10 121208012 intergenic variant C/T snv 0.72 2
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs1076064
PPARGC1B ; MIR378A
0.851 0.160 5 149732603 intron variant A/G snv 0.47 4
rs10761581
NCOA4
0.925 0.080 10 46027444 missense variant A/C snv 0.44 0.41 2
rs10763567 1.000 0.080 10 46057653 regulatory region variant G/A;T snv 1
rs10773338
LINC02405
0.925 0.080 12 126919857 intron variant G/A;T snv 2
rs10774740 1.000 0.080 12 114228397 intergenic variant G/A;T snv 1
rs10788165 0.925 0.080 10 121284700 regulatory region variant T/G snv 0.35 2
rs10793821 1.000 0.080 5 134500518 upstream gene variant C/A;T snv 0.62 1
rs10845938 1.000 0.080 12 14263984 intergenic variant A/G snv 0.52 1