Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6682925
C1orf141 ; IL23R
0.776 0.160 1 67165579 intron variant C/T snv 0.47 11
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 10
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs1234314
TNFSF4
0.790 0.320 1 173208253 upstream gene variant C/A;G snv 7
rs12566888
PEAR1
0.807 0.280 1 156899255 intron variant G/T snv 0.26 7
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 7
rs1044925
SOAT1
0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs12746200
PLA2G4A
0.851 0.160 1 186880054 intron variant A/G snv 7.3E-02 6
rs2306235
PLEKHO1
0.827 0.040 1 150150942 missense variant C/G;T snv 1.1E-02; 1.6E-05 4.4E-03 6
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs5177
LRP8
0.851 0.120 1 53246063 3 prime UTR variant G/A;C snv 6
rs7211
TXNIP
0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs142648132
MTR
0.827 0.160 1 236816521 missense variant G/A;C;T snv 8.4E-04; 2.4E-05 5
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5