Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs1524107
IL6-AS1 ; IL6
0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02 6
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs2237897
KCNQ1
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 6
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
rs387906536
LYZ
0.851 0.200 12 69350215 missense variant T/A;C snv 6
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs702553
PDE4D
0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs869025495
NPHS2
0.851 0.080 1 179564715 missense variant G/A snv 6
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs2412971
HORMAD2
0.882 0.320 22 30098382 intron variant G/A snv 0.55 5
rs267606743
COL4A1
1.000 0.160 13 110192222 missense variant C/T snv 5
rs8177412
GPX3 ; LOC105378228
0.851 0.160 5 151020526 5 prime UTR variant T/C snv 0.15 5
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs841853
SLC2A1
0.882 0.200 1 42935767 intron variant A/C snv 0.66 4
rs1191455921
LMX1B
0.925 0.240 9 126693319 missense variant G/A snv 3
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs136161
APOL1
0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs1883414
HLA-DPB2
0.925 0.200 6 33118671 non coding transcript exon variant G/A snv 0.28 3
rs2607420
ITPKC
0.925 0.120 19 40738982 intron variant G/A snv 0.76 3
rs28362930
SEMA7A
0.925 0.160 15 74408859 downstream gene variant G/A snv 0.16 3
rs4972593
LOC107985961
0.925 0.200 2 173598126 intergenic variant T/A snv 0.20 3
rs741301
ELMO1
0.925 0.160 7 36878390 intron variant C/T snv 0.59 3