Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs2145270 20 6641038 regulatory region variant C/T snv 0.61 4
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 4
rs3812049
SLC12A2 ; LINC01184
5 128083158 non coding transcript exon variant C/A;G;T snv 4
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 4
rs17511102
LOC105374465 ; CDC42EP3
2 37733470 intron variant A/G;T snv 3
rs3817428
ACAN
15 88872016 missense variant C/G snv 0.20 0.20 3
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs41310284 10 100687890 intergenic variant C/A;T snv 3
rs994014 4 81244636 intergenic variant T/C snv 0.43 3
rs12820906
PITPNM2
12 123008576 intron variant A/G snv 0.20 2
rs28584580
ACAN
15 88854596 intron variant A/G snv 0.11 2
rs3027009
ACKR1 ; CADM3-AS1
1 159204097 intron variant A/G snv 5.8E-02 2
rs35344761
PCSK5
9 75895907 intron variant C/A snv 0.10 2
rs465983
C5orf67
5 56516303 intron variant A/G snv 0.27 2
rs4694504 4 72630974 intergenic variant A/G;T snv 2
rs481806
JAZF1
7 28167681 intron variant G/T snv 0.77 2
rs4846204
KIF1B
1 10248900 intron variant C/T snv 9.3E-02 2
rs6492538 13 91341492 intergenic variant A/C snv 0.83 2
rs7306275 12 49856328 upstream gene variant G/A snv 0.29 2
rs798491
AMZ1 ; GNA12
7 2760887 intron variant A/C;G snv 2
rs9358913
H4C6
6 26239176 upstream gene variant A/G snv 0.24 2
rs991967
TGFB2-OT1 ; TGFB2
1 218442109 3 prime UTR variant A/C snv 0.37 2
rs10402308
CILP2
19 19546691 downstream gene variant G/A snv 0.27 1
rs10584116
AFG3L1P
16 89995916 non coding transcript exon variant CT/- delins 0.14 1