Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs20417
PACERR ; PTGS2
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs5065
NPPA ; CLCN6 ; NPPA-AS1
0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv 9
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs4444878
F11-AS1
0.851 0.120 4 186292729 intron variant C/A;T snv 7
rs1906591 0.851 0.200 4 110787733 intergenic variant G/A snv 0.15 5
rs761740955
FGB
0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 5
rs13143308 0.882 0.120 4 110793263 upstream gene variant T/C;G snv 4
rs2910829
PDE4D
0.925 0.080 5 60174072 intron variant G/A snv 0.52 3
rs152312
PDE4D ; PART1
0.925 0.080 5 60491989 non coding transcript exon variant G/A;T snv 3
rs12932445
ZFHX3
0.925 0.080 16 73035989 intron variant T/C snv 0.18 3
rs6891174 0.925 0.040 5 173213587 intergenic variant A/G snv 0.73 2
rs5067
CLCN6 ; NPPA ; NPPA-AS1
0.925 0.080 1 11845924 3 prime UTR variant A/G;T snv 0.21 2
rs1003346
TMEM245
1.000 9 109053060 intron variant C/A snv 0.43 2
rs16939239 1.000 8 76122993 intergenic variant G/A snv 0.14 1
rs638704 1.000 1 170629046 intron variant C/T snv 0.64 1
rs2257073
ASB10
1.000 7 151186200 intron variant C/T snv 0.26 1
rs4727833
CAV2
1.000 7 116507854 3 prime UTR variant C/G;T snv 1
rs11596587
HK1
1.000 10 69354232 intron variant C/T snv 0.11 1
rs2273235
NDST1
1.000 5 150527971 synonymous variant T/G snv 0.45 0.42 1