Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs939348
THRA
0.851 0.240 17 40075600 intron variant T/C;G snv 5
rs9385284 6 123078960 intergenic variant A/G snv 0.24 3
rs9381299 6 44244130 upstream gene variant T/C snv 0.15 1
rs9375813
LOC105378005
6 131436107 intergenic variant C/A snv 0.14 2
rs9375459 6 126826559 intron variant C/T snv 0.39 1
rs9350602
MYO6
6 75850781 intron variant C/T snv 0.13 1
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs9332982
CYP4A11
1 46940506 intron variant G/A snv 8.8E-02 1
rs9332978
CYP4A11
0.882 0.040 1 46942278 upstream gene variant T/C snv 7.3E-02 5
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs928554
ESR2
0.851 0.120 14 64227477 3 prime UTR variant C/T snv 0.66 6
rs920435389
FGFR4
1.000 0.040 5 177091064 missense variant G/C snv 3
rs911154679
AGTR1
1.000 0.040 3 148741352 missense variant C/T snv 7.0E-06 2
rs909656
APLN
X 129648585 intron variant G/A;T snv 1.4E-02 1
rs897876 0.882 0.040 2 65564447 intron variant C/T snv 0.30 4
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs891512
NOS3
0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 4
rs891511
NOS3
7 151007755 intron variant G/A;C snv 4
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs876537
CRPP1
1.000 0.080 1 159705143 non coding transcript exon variant C/T snv 0.34 3
rs8702
KLC1
0.851 0.160 14 103686015 3 prime UTR variant C/G snv 0.61 5
rs867593888
MYH9
0.882 0.200 22 36292059 missense variant T/C snv 11
rs866528738
POU2F3
1.000 0.080 11 120302360 missense variant G/A snv 2