Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1894111
GRK2
11 67271141 intron variant T/C snv 0.95 1
rs275646 3 148745735 downstream gene variant T/C snv 0.95 1
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs4536
GML ; CYP11B2
8 142914345 synonymous variant C/T snv 0.90 0.94 1
rs6461992
HOXA10-HOXA9 ; HOXA11 ; HOXA10
1.000 0.120 7 27181212 3 prime UTR variant A/G snv 0.93 5
rs4722675
HOTTIP
7 27204343 intron variant A/G snv 0.93 4
rs10033366
ENPEP
4 110409934 intron variant T/C snv 0.92 1
rs1991517
LOC101928462 ; TSHR
0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 13
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs6453204
SV2C
1.000 0.080 5 76143375 intron variant A/G snv 0.90 2
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs16827043 1 146039555 upstream gene variant C/T snv 0.89 1
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs316019
SLC22A2
0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs2272592
DDAH2 ; CLIC1
1.000 0.080 6 31730575 5 prime UTR variant T/C snv 0.88 2
rs4425
TBC1D22A
22 46903089 intron variant T/C snv 0.88 1
rs2070008
FGA
4 154592124 upstream gene variant C/T snv 0.88 1
rs7406910
HOXB7
17 48610894 missense variant T/C snv 0.88 0.88 3
rs2198596
SGCZ
8 15143257 intron variant G/C snv 0.87 1
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 4
rs1656930 1.000 0.080 3 186835068 intergenic variant A/G snv 0.86 3
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs891512
NOS3
0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 4
rs2469997 8 119341027 intergenic variant G/C snv 0.83 2