Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036128
LINC02196
5 6937069 intron variant G/A;C;T snv 1
rs1008924
FRMD6
14 51616362 intron variant G/A snv 0.47 1
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 5
rs10235512
RADIL
7 4865424 intron variant T/C;G snv 1
rs10255299
DOCK4
7 111887504 intron variant G/A snv 0.11 2
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10429953
CR1
1 207615233 intron variant A/G snv 0.19 1
rs10435719 8 11919395 downstream gene variant C/T snv 0.48 2
rs10437339 1 159740595 intergenic variant C/G;T snv 1
rs10437340 1 159741019 intergenic variant G/C snv 0.40 1
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 3
rs10489849 1 159226975 regulatory region variant C/A;T snv 1
rs10494326 1 159679910 intergenic variant C/T snv 5.3E-02 1
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 4
rs1051338
LIPA
0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 7
rs10518765
UNC13C
1.000 0.040 15 54388434 intron variant A/C snv 0.16 3
rs10521222 16 51124799 intergenic variant C/T snv 3.2E-02 1
rs10744775
BRAP
12 111658411 intron variant T/C snv 0.44 2
rs10745954
C12orf42
12 103089316 intron variant A/G snv 0.60 1
rs10751037 11 81025386 intron variant C/G;T snv 1
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs10774579
HNF1A-AS1
12 120967407 intron variant T/C snv 0.43 1
rs10774580
OASL
12 121038620 intron variant A/G snv 0.55 1
rs10778213
C12orf42
12 103101373 intron variant T/C snv 0.57 1
rs10778215
C12orf42
12 103143488 intron variant T/A;G snv 2