Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs17779747 1.000 0.040 17 70498851 regulatory region variant G/T snv 0.24 2
rs386418 1.000 0.040 Y 3213255 intergenic variant G/C snv 1
rs7208480 1.000 0.040 17 15770470 non coding transcript exon variant C/T snv 0.28 1
rs876188 1.000 0.040 14 98012267 intergenic variant G/A snv 0.66 1
rs73598374
ADA
0.790 0.280 20 44651586 missense variant C/A;G;T snv 7.1E-06; 6.2E-02 8
rs3730070
ADCY6
0.925 0.120 12 48775065 intron variant G/C snv 0.13 0.23 2
rs1208917022
ATN1
1.000 0.040 12 6936663 missense variant A/G snv 3
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs1427407
BCL11A
0.827 0.120 2 60490908 intron variant T/C;G snv 6
rs149767043
C20orf194
1.000 0.040 20 3343726 missense variant G/C snv 4.0E-06 7.0E-06 1
rs786205745
CACNA1C
0.807 0.320 12 2504538 missense variant G/A;C snv 6
rs79891110
CACNA1C
0.807 0.320 12 2504944 stop gained G/A;T snv 6
rs587782933
CACNA1C
0.827 0.200 12 2504526 missense variant G/A snv 5
rs786205753
CACNA1C
0.925 0.080 12 2593255 missense variant G/A snv 3
rs80315385
CACNA1C
0.882 0.200 12 2504932 missense variant G/A snv 3
rs192749597
CACNA1C ; CACNA1C-AS1
0.882 0.080 12 2679712 missense variant C/T snv 9.2E-04 3.5E-03 3
rs755221106
CACNA1G
0.851 0.040 17 50617560 missense variant G/A;T snv 4.0E-06 7
rs267607277
CALM1
0.807 0.120 14 90404386 missense variant A/G snv 6
rs398124647
CALM2
0.807 0.120 2 47161851 missense variant T/A;C snv 6
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs3734960
DPP6
0.925 0.240 7 154892443 missense variant T/C snv 0.33 0.36 2
rs730880082
DSP
0.882 0.120 6 7576986 stop gained C/G;T snv 3
rs587777598
ELOVL4
0.851 0.200 6 79921662 missense variant C/G;T snv 4
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102