Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs9901675
CD68 ; LOC100996842
17 7581494 missense variant G/A snv 5.4E-02 5.5E-02 5
rs12150660
SHBG
1.000 0.040 17 7618597 intron variant G/T snv 0.17 5
rs6258
SHBG
1.000 0.040 17 7631360 missense variant C/A;T snv 5.6E-05; 4.5E-03 5
rs10454142 2 48419260 intergenic variant T/C snv 0.22 3
rs10514317 5 89813933 intergenic variant C/A;T snv 3
rs1573036 X 110576840 intergenic variant C/T snv 0.42 3
rs1641537 17 7642403 upstream gene variant T/C snv 0.75 3
rs17496332 1 107003753 intergenic variant A/G snv 0.26 3
rs293428 4 68726064 intergenic variant A/G snv 0.36 3
rs440837 8 80549739 intergenic variant A/G snv 0.39 3
rs3779195
BAIAP2L1
7 98364050 intron variant T/A snv 0.16 3
rs7910927
JMJD1C
10 63379150 intron variant T/A;G snv 3
rs2411984
LOC102724596
17 49368389 intron variant G/A snv 0.18 3
rs8023580
LOC112268156 ; NR2F2-AS1
15 96165062 intron variant T/C snv 0.29 3
rs2075230
MPDU1 ; LOC100996842
17 7583790 5 prime UTR variant A/C;G snv 4.0E-06; 0.19 3
rs9635963
OSBPL1A
18 24169651 intron variant G/A snv 0.60 1
rs6761
POLR2A
17 7514346 non coding transcript exon variant C/T snv 0.55 1