Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200550971
CNR1
0.925 0.040 6 88144985 missense variant T/C snv 3.6E-05 1.4E-05 3
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18 5
rs55808324
GALC
14 87978408 intron variant G/A snv 0.19 1
rs9282564
ABCB1
1.000 0.080 7 87600124 missense variant T/A;C;G snv 7.3E-02 7.3E-02 2
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs6592362
LOC107984361
11 87414396 intergenic variant A/G snv 0.69 1
rs11641016 16 85981275 intron variant C/G snv 0.18 1
rs16940202 1.000 0.040 16 85980635 intron variant T/C snv 0.15 2
rs10521318 16 85977731 intron variant C/G;T snv 1
rs4552569 1.000 0.040 5 83877774 upstream gene variant C/T snv 0.75 2
rs778180128
CYBC1
17 82449249 stop gained G/C snv 1
rs11548656
PLCG2
1.000 0.040 16 81883307 missense variant A/G snv 2.5E-02 2.7E-02 2
rs72634258 1 8090578 intron variant T/C snv 0.13 1
rs16953946
CDYL2
16 80751551 intron variant T/A;C snv 1
rs6586030
TSPAN14
1.000 0.040 10 80494291 intron variant A/G;T snv 2
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv 6
rs950318 3 80354036 intergenic variant C/G snv 0.22 1
rs721917
SFTPD
0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs2243639
SFTPD
0.882 0.080 10 79941966 missense variant T/C;G snv 0.66 4
rs3766606
PARK7
0.827 0.120 1 7962137 intron variant G/T snv 0.22 6
rs35675666
PARK7
1.000 0.040 1 7961913 5 prime UTR variant G/C;T snv 2
rs7236492
NFATC1 ; LOC101927897
0.827 0.120 18 79460616 non coding transcript exon variant C/T snv 0.11 6