Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2887915 2 210689850 intergenic variant C/G;T snv 1
rs500456 7 54531089 intergenic variant A/G snv 0.47 1
rs7195832 16 19947804 intergenic variant T/A snv 1
rs883484 9 122362748 intergenic variant C/T snv 0.20 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs478333
ABCB11
2 168922646 3 prime UTR variant G/A snv 0.46 1
rs3764913
ACADL
1.000 0.080 2 210210185 non coding transcript exon variant T/C snv 0.30 0.27 3
rs1799958
ACADS
0.882 0.160 12 120738280 missense variant G/A snv 0.26 0.21 4
rs2014355
ACADS
0.925 0.120 12 120737721 non coding transcript exon variant T/C snv 0.22 4
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs762533455
ADRB2
5 148827300 missense variant G/A snv 4.0E-06 1
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs12721226
AGTR1
3 148741522 missense variant G/A snv 6.3E-04 1.6E-04 1
rs6546837
ALMS1
2 73450771 missense variant G/C;T snv 0.27 1
rs375811360
ALMS1P1 ; NAT8
1.000 0.080 2 73643197 intron variant C/G snv 2
rs3803278
ALOX5AP
13 30744264 non coding transcript exon variant T/C snv 0.20 1
rs2074379
ALPK1
1.000 4 112431743 missense variant G/A snv 0.62 0.65 3
rs2074388
ALPK1
1.000 4 112431241 missense variant G/A snv 0.62 0.65 3
rs2074380
ALPK1
4 112432155 missense variant G/A;T snv 8.5E-03; 2.4E-05 2
rs2074381
ALPK1
4 112432293 missense variant A/G snv 8.5E-03 5.5E-03 2