Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11110004
ANKS1B
1.000 0.040 12 99694540 intron variant T/C snv 5.1E-03 3
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14 3
rs16867253
GRHL1
0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 7
rs12362161 1.000 0.040 11 98834502 intergenic variant C/A;G snv 3
rs16917667
C8orf37-AS1
1.000 0.040 8 95439600 intron variant G/A snv 4.1E-02 3
rs74864598
C8orf37-AS1
1.000 0.040 8 95439207 intron variant C/A snv 4.4E-02 3
rs762151808
SERPINA1
0.925 0.040 14 94378559 missense variant A/C snv 4.0E-06 7.0E-06 2
rs370579379
RBP4 ; FFAR4
0.827 0.160 10 93594018 missense variant C/T snv 4.0E-06 1.4E-05 6
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs149322277
CA5A
1.000 0.040 16 87925065 intron variant C/T snv 5.6E-03 3
rs1700575
LOC105374647
1.000 0.040 5 8543925 intron variant A/T snv 0.26 3
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs2549513
MAF
0.851 0.080 16 79516830 downstream gene variant C/A;T snv 4
rs991104525
ARSB
0.882 0.160 5 78969051 missense variant G/A snv 1.2E-05 7.7E-05 4
rs8179090
TIMP2
0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 12
rs7965830
LOC105369844
1.000 0.040 12 75962050 intron variant C/A;T snv 3
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs28763958
DSP
0.882 0.080 6 7558186 missense variant A/G snv 6.4E-05 2.8E-05 3
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs548097 1.000 0.040 13 75202132 intergenic variant G/C;T snv 1
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16