Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10033366
ENPEP
4 110409934 intron variant T/C snv 0.92 1
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs10046
MIR4713HG ; CYP19A1
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs10050860
ERAP1
0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16 4
rs10069554 5 33204354 intron variant T/C snv 0.45 1
rs10086846
CYP11B2 ; GML
8 142915715 intron variant C/A;T snv 1
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs1012657750
SELENBP1
1 151368294 missense variant G/C snv 2
rs1012841819
ADRA2B
0.882 0.160 2 96115728 missense variant G/A snv 4.0E-06 4
rs10184428 2 164155317 intron variant C/A;G snv 5
rs10188442
GPR39
2 132431666 intron variant C/T snv 0.22 1
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs1024323
GRK4
0.882 0.160 4 3004316 missense variant C/A;G;T snv 0.36 4
rs1027989
LYN
8 55901862 intron variant G/A;C snv 3
rs10279895 7 27288591 intergenic variant A/G snv 2.9E-02 1
rs1037733674
GCG ; LOC101929532
0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs1042039
XDH
2 31335440 3 prime UTR variant T/C snv 0.41 1
rs1042309696
ACE
17 63487006 synonymous variant T/C snv 2
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54