Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs10494132
CHIA
0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 4
rs12123821
LOC112268240 ; FLG-AS1
0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 4
rs2070901
FCER1G
0.882 0.120 1 161215268 non coding transcript exon variant G/T snv 0.32 4
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs7518129
TNFSF4
0.882 0.120 1 173194429 intron variant A/G snv 0.47 3
rs10158467 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 2
rs10924993 0.925 0.080 1 236296485 intergenic variant T/A;G snv 2
rs12023876
ADORA1
0.925 0.080 1 203124073 intron variant G/A;T snv 2
rs12081541 0.925 0.160 1 152468890 intergenic variant T/C snv 8.9E-02 2
rs1617333
CD247
0.925 0.080 1 167467033 intron variant A/G snv 0.27 2
rs67551275
SPSB1
0.925 0.080 1 9296617 intron variant T/C snv 0.43 2
rs78037977 0.925 0.120 1 172746562 upstream gene variant A/G snv 7.9E-02 2
rs12750027
FLVCR1
1.000 0.080 1 212883085 intron variant G/A snv 4.3E-02 1
rs2289447
ATPAF1
1.000 0.080 1 46652496 non coding transcript exon variant C/G;T snv 1
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 4
rs143326447
MIR4435-2HG ; SOCAR
0.925 0.080 2 111511155 intron variant T/C snv 0.11 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs13416555
LINC00299
1.000 0.080 2 8301605 intron variant C/A;G snv 3
rs3856439
LINC00299
0.925 0.080 2 8319274 intron variant C/A;T snv 0.29 3
rs10187276 0.925 0.080 2 227805721 upstream gene variant T/C snv 0.62 2
rs142320277
LRP1B
1.000 0.080 2 140665410 intron variant G/A;C snv 2
rs1861245
IL18R1 ; IL1RL1
0.925 0.080 2 102350446 intron variant C/T snv 2