Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12056222 7 9700008 intron variant A/C snv 0.39 1
rs12187548 5 143483182 intergenic variant A/C snv 0.66 1
rs12199656
REV3L ; MFSD4B
6 111353940 non coding transcript exon variant A/C snv 0.11 1
rs12209322
GMDS-DT
6 2436931 intron variant A/C snv 0.23 1
rs12274157
DAGLA
11 61710175 intron variant A/C snv 0.17 1
rs12472491 2 106573081 regulatory region variant A/C snv 0.17 1
rs12477908 2 27764179 intergenic variant A/C snv 0.62 1
rs12598215 16 48856564 intergenic variant A/C snv 0.85 1
rs12769144
DPCD
10 101609797 downstream gene variant A/C snv 7.6E-02 1
rs12995461
C2orf16
2 27555300 intron variant A/C snv 0.23 1
rs1328501 9 80553196 regulatory region variant A/C snv 0.65 1
rs1367104 8 40502376 intergenic variant A/C snv 0.70 1
rs1542270 8 57580266 intron variant A/C snv 0.74 1
rs1558860 11 116736652 regulatory region variant A/C snv 0.93 1
rs1640980
ABAT
16 8709764 intron variant A/C snv 0.68 1
rs16846817
LOC107985779 ; LRP1B
2 141672738 intron variant A/C snv 0.13 1
rs16940181
ALDH1A2
15 58395325 intron variant A/C snv 0.13 1
rs17000260 4 75108576 intergenic variant A/C snv 9.6E-02 1
rs174461
FADS3
11 61889929 intron variant A/C snv 0.59 1
rs1748201
DOCK7
1 62579835 intron variant A/C snv 0.57 1
rs17663278
SLC16A10
6 111183678 intron variant A/C snv 0.10 1
rs17821316
ALDH1A2 ; LIPC
15 58410870 intron variant A/C snv 0.41 1
rs2047103 12 74590330 intergenic variant A/C snv 0.66 1
rs2074901
CYP4F2
19 15886612 intron variant A/C snv 0.14 1
rs2154408
LOC728755
14 27528973 intron variant A/C snv 0.62 1