Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 6
rs34214527
TNXB
0.925 0.040 6 32046679 intron variant C/T snv 0.11 6
rs613872
TCF4
0.851 0.120 18 55543071 intron variant G/T snv 0.88 6
rs16978075
LINC01478 ; LINC01601
18 44533186 intron variant T/C snv 8.5E-02 5
rs198806
H2AC6
0.925 0.120 6 26133388 intron variant A/G snv 0.59 4
rs2093210
C14orf39
1.000 0.040 14 60490561 intron variant C/T snv 0.45 4
rs2629540
FAM53B
0.925 0.080 10 124737579 intron variant G/C snv 0.18 4
rs642803
OVOL1
0.925 0.120 11 65793149 intron variant C/T snv 0.42 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs71636784
ZDHHC18
1.000 0.040 1 26842709 intron variant T/G snv 0.12 4
rs7832708
MSRA
8 10332530 intron variant C/T snv 0.49 4
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42 4
rs10752262
CAMK1D
1.000 0.040 10 12353101 intron variant C/T snv 0.39 3
rs1149558
EXOC4
0.925 0.080 7 133363002 intron variant T/C;G snv 3
rs1167800
HIP1
7 75546898 intron variant A/G snv 0.34 3
rs11765189
PTPRN2
1.000 0.040 7 157743285 intron variant A/G snv 0.25 3
rs12602286
EPN2
1.000 0.040 17 19333641 intron variant G/T snv 0.79 3
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs2668196
BCHE
3 165784921 intron variant A/T snv 0.75 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs4396807
TRIOBP
22 37742372 intron variant G/C snv 0.38 3
rs6119267
NOL4L-DT ; NOL4L
20 32576112 intron variant C/A;G snv 3
rs62154720
TGFBRAP1
1.000 0.040 2 105306623 intron variant C/T snv 9.2E-02 3
rs6870983
TMEM161B-AS1
5 88401716 intron variant C/T snv 0.29 3
rs7218708
SPECC1
17 20023523 intron variant A/C;G snv 3