Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs10995311
ADO
10 62805174 missense variant C/G snv 0.35 0.31 3
rs112607182 3 170309619 downstream gene variant C/T snv 5.3E-02 2
rs17158386 7 29765745 regulatory region variant G/A snv 0.19 2
rs2236295
ADO
10 62805132 missense variant G/C;T snv 0.32 2
rs6535594
NR3C2
4 148211605 intron variant G/A snv 0.54 2
rs67339103
LRMDA
10 76133928 intron variant G/A;C;T snv 2
rs10157710 1 47496019 downstream gene variant C/T snv 0.78 1
rs10207567
ICA1L
2 202850250 intron variant G/A;C snv 1
rs11162351
AK5
1 77479047 intron variant C/G snv 0.31 1
rs1124694
LINC02752
11 11077129 intron variant A/G;T snv 1
rs11264327 1 155122631 downstream gene variant G/A;C;T snv 1
rs1145074
SPATA5L1
15 45411626 intron variant T/A;G snv 0.45 1
rs12032996 1 33454985 intergenic variant G/A snv 0.12 1
rs12727104 1 171454028 intergenic variant G/A snv 8.3E-02 1
rs12727980
LINC00862
1 200289967 intron variant C/T snv 0.54 1
rs1276720
CUBN
10 16929427 intron variant C/T snv 0.65 1
rs13394343 2 85527219 intergenic variant C/A;T snv 1
rs141640975
CUBN
10 16950012 missense variant G/A snv 1.7E-03 1.5E-03 1
rs144360241
CUBN
10 16925418 missense variant T/C snv 5.6E-03 5.3E-03 1
rs144994089
AQP7
9 33385158 missense variant C/T snv 7.0E-04 8.2E-04 1
rs16943246 15 45428399 upstream gene variant G/A snv 0.29 1
rs17368443
SBF2
11 10275289 intron variant G/C snv 5.3E-02 1
rs183131780
LOC105373914 ; LOC107985992
2 225820170 intergenic variant C/T snv 1.0E-03 1
rs185291443 2 226120788 intergenic variant C/A;G snv 1