Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 11
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 10
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 10
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 8
rs8037137
RCCD1
0.807 0.160 15 90963407 upstream gene variant T/C snv 0.19 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs342293
CTB-30L5.1
0.882 0.040 7 106731773 intron variant C/G snv 0.42 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 6
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 6