Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10838687
MADD
11 47291341 intron variant T/G snv 0.31 2
rs10891343
BCO2
11 112209661 intron variant T/C snv 0.44 2
rs10908713 1 159369769 intron variant T/C snv 0.47 2
rs11208722 1 65705318 intron variant C/A snv 0.75 2
rs11265174 1 159350569 intron variant T/A snv 0.35 2
rs11265190
OR10J1
1 159421611 intron variant G/A snv 0.47 2
rs11265191
OR10J1 ; OR10J4
1 159430569 intron variant C/G;T snv 2
rs11265196 1 159448422 intron variant G/A snv 0.47 2
rs11265263 1 159740727 intergenic variant C/A;T snv 2
rs1127311
ADAR ; CHRNB2
1 154584187 3 prime UTR variant G/A snv 0.42 2
rs116971887
LOC105371253 ; SALL1
16 51136115 3 prime UTR variant G/T snv 3.1E-02 2
rs11874381
LOC105372112
18 49677038 intergenic variant G/A snv 0.32 2
rs12034598
CR1
1 207584170 intron variant A/G snv 0.19 2
rs12034864 1 159215190 regulatory region variant A/C;G;T snv 2
rs12034969
OR10J1
1 159415154 intron variant T/C snv 0.46 2
rs12047230 1 159509215 intergenic variant A/G snv 0.33 2
rs12072644 1 159245497 intergenic variant C/A;T snv 2
rs12711751 2 113080188 downstream gene variant T/G snv 0.61 2
rs12739022 1 159689641 intergenic variant T/C snv 0.24 2
rs12742376
KDF1
1 26958704 intron variant C/T snv 6.8E-02 2
rs12754915 1 159691079 intergenic variant T/C snv 0.25 2
rs12755606 1 159700546 downstream gene variant C/G snv 0.24 2
rs13409360 2 113080525 downstream gene variant G/A snv 0.38 2
rs1441759 8 20008052 intergenic variant G/C snv 2.9E-02 2
rs1584252 1 159553838 upstream gene variant A/T snv 0.30 2