Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10249651
ASZ1 ; CFTR
1.000 0.040 7 117424571 intron variant T/C snv 0.40 1
rs10267593
MAD1L1
1.000 0.040 7 1897625 intron variant G/A snv 0.25 1
rs1034246
PTK7
1.000 0.040 6 43100632 intron variant G/T snv 0.19 1
rs1035071612
MIR6886 ; LDLR
0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
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
rs1044925
SOAT1
0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10456100
KCNK5
1.000 0.040 6 39215694 intron variant C/T snv 0.20 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1048990
PSMA6
0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs1049255
CYBA
0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10495907 1.000 0.040 2 43771587 upstream gene variant G/A snv 0.13 1
rs1049673
CD36
0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs1050286
OLR1
0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40 3
rs1050362
DHX38
1.000 0.040 16 72096916 missense variant C/A;T snv 0.38; 2.4E-05 1
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10509681
CYP2C8
0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 8