Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs11171739
ERBB3
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 10
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs2279574
DUSP6
0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 8
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 7
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 6
rs613872
TCF4
0.851 0.120 18 55543071 intron variant G/T snv 0.88 6
rs34214527
TNXB
0.925 0.040 6 32046679 intron variant C/T snv 0.11 6
rs2515919 1.000 6 31596390 upstream gene variant A/G snv 0.31 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs16978075
LINC01478 ; LINC01601
18 44533186 intron variant T/C snv 8.5E-02 5
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 5
rs13212562 0.925 0.120 6 27332531 intergenic variant A/G snv 0.13 4
rs2093210
C14orf39
1.000 0.040 14 60490561 intron variant C/T snv 0.45 4
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42 4
rs2629540
FAM53B
0.925 0.080 10 124737579 intron variant G/C snv 0.18 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs198806
H2AC6
0.925 0.120 6 26133388 intron variant A/G snv 0.59 4
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
rs7832708
MSRA
8 10332530 intron variant C/T snv 0.49 4
rs642803
OVOL1
0.925 0.120 11 65793149 intron variant C/T snv 0.42 4
rs71636784
ZDHHC18
1.000 0.040 1 26842709 intron variant T/G snv 0.12 4
rs78381888
ANKRD23 ; CNNM3
0.925 0.040 2 96835038 3 prime UTR variant A/G snv 0.13 3
rs72829446
ATP1B2
17 7648805 intron variant C/T snv 6.5E-02 3