Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2328546
CDKAL1
6 20657114 intron variant T/C snv 0.81 1
rs2341557
PLXNA4
7 132134524 intron variant T/C snv 0.56 1
rs2395022
KPNA7
7 99152756 intergenic variant A/C snv 0.93 1
rs2412970
HORMAD2
22 30090837 intron variant A/G snv 0.55 1
rs2427870 X 136581905 upstream gene variant C/T snv 0.52 1
rs2472649 4 73991991 upstream gene variant A/G;T snv 1
rs2593855
FOXP1
3 71126344 intron variant C/T snv 0.30 1
rs273506
MAST3
19 18110837 intron variant C/A;T snv 1
rs2790216
IPMK
10 58238165 intron variant G/A snv 0.34 1
rs2839073 21 45953845 regulatory region variant T/C snv 0.16 1
rs2847278 18 12778716 upstream gene variant C/T snv 0.83 1
rs304496
LIPA
10 89387005 intron variant A/G snv 0.96 1
rs34688635
NOX1
X 100850206 missense variant C/T snv 1.9E-02 2.0E-02 1
rs34694289
FCER2
19 7689215 missense variant G/A;C snv 2.4E-03; 1.6E-05 1
rs34856868
BTBD8
1 92088726 missense variant G/A snv 2.0E-02 2.0E-02 1
rs35730213
INAVA
1 200905101 intron variant G/C snv 0.22 1
rs36221701
SMAD3 ; LOC102723493
15 67064151 non coding transcript exon variant T/C;G snv 1
rs3766920
LOC101928120 ; SHC1 ; PYGO2
1 154962487 3 prime UTR variant G/A snv 1.2E-03 1
rs3798544
SPDEF
6 34552490 intron variant G/A snv 0.24 1
rs4317455
PSMG4
6 3263257 intron variant C/T snv 0.68 1
rs444210
LOC105378120
6 166976754 intron variant A/G snv 0.44 1
rs4821558
CSF2RB
22 36912743 upstream gene variant T/C snv 0.20 1
rs4836519 5 130681594 intron variant T/A;C snv 1
rs4899554 14 75234518 downstream gene variant C/T snv 0.14 1
rs490608
DAP3
1 155713079 intron variant C/T snv 0.48 1