Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs2071449
HOXC4 ; HOXC5 ; MIR615
12 54034227 intron variant C/A;T snv 0.35; 4.2E-06 4
rs2638953
CCDC91
12 28381482 intron variant G/C;T snv 4
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 4
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs7697556 4 72649596 intergenic variant T/A;C snv 4
rs7773004 1.000 0.040 6 26267527 downstream gene variant A/C;G;T snv 4
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs113029345 19 40864271 intron variant T/C snv 3
rs117582141 10 92804854 intergenic variant T/A;C snv 3
rs12608504 19 18278325 upstream gene variant A/G;T snv 3
rs12903295
IREB2
15 78486630 intron variant A/C;G;T snv 3
rs12910627
LOC112268142 ; CHRNB4 ; LOC105370913
15 78702591 intron variant G/A;C snv 3
rs1504550
IREB2
15 78473908 3 prime UTR variant A/G;T snv 3
rs17396340
KIF1B
1 10226118 intron variant G/A;C snv 3
rs17405217
IREB2
15 78438807 non coding transcript exon variant C/G;T snv 3
rs17483929
IREB2
15 78450034 intron variant G/A;T snv 3
rs17484235
IREB2
15 78469072 intron variant C/A;G;T snv 3
rs4765219
CCDC92
12 123955563 intron variant C/A;T snv 3
rs4947642 7 51797912 intergenic variant A/C;G snv 3
rs569207
CHRNA5
15 78580777 intron variant C/G;T snv 0.34 3
rs6090583
EYA2
20 46930192 intron variant A/C;G snv 3
rs754133
HOXC6 ; HOXC4 ; HOXC5
12 54025136 intron variant G/A;C snv 3
rs7917772
SFXN2
10 102727686 3 prime UTR variant G/A;C snv 0.46 3