Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4804411
INSR
19 7222366 intron variant G/A;C snv 3
rs57457691
PEPD
19 33420799 intron variant T/C snv 0.62 3
rs143020224
SMARCA4
19 11076648 intron variant C/G;T snv 2
rs28873836
FPR3 ; ZNF577
19 51811402 intron variant G/A;C snv 2
rs367070 19 54296648 upstream gene variant G/A snv 0.81 2
rs142673685 19 31669942 intergenic variant C/T snv 4.0E-03 1
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 6
rs1943940 18 74037957 upstream gene variant T/C snv 0.42 3
rs58084604 18 60182196 intergenic variant C/T snv 0.24 3
rs140520944 18 29508647 intergenic variant G/T snv 4.7E-03 1
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs11870935
KPNB1
17 47655239 intron variant G/A;C snv 4
rs4277405 17 63471557 upstream gene variant C/T snv 0.63 4
rs8071884
PGS1
17 78401977 intron variant C/A;G;T snv 4
rs881844
STARD3
0.925 0.080 17 39653965 intron variant C/G snv 0.51 4
rs8178824
APOH
17 66228657 intron variant C/T snv 2.3E-02 3
rs117753190
ABCA6
17 69140184 intron variant C/G snv 2.0E-02 2
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs62033406
FTO
16 53790314 intron variant A/G snv 0.33 5
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs3743832
C16orf72
1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs3794695
HPR ; TXNL4B
16 72063928 intron variant C/A;T snv 4