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
rs727479
MIR4713HG ; CYP19A1 ; MIR4713
0.790 0.240 15 51242350 intron variant C/A;T snv 10
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
rs2445762
CYP19A1
1.000 0.080 15 51325511 intron variant T/C snv 0.31 4
rs2414095
CYP19A1 ; MIR4713HG
15 51232095 intron variant A/G snv 0.69 4
rs12591359
MIR4713HG ; CYP19A1
0.925 0.080 15 51247171 intron variant G/A snv 0.41 4
rs10454142 2 48419260 intergenic variant T/C snv 0.22 3
rs10514317 5 89813933 intergenic variant C/A;T snv 3
rs12751297 1 242792261 intergenic variant G/A 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
rs36019094 5 40237272 upstream gene variant C/A snv 3
rs3849221 9 135136831 regulatory region variant A/C snv 0.59 3
rs440837 8 80549739 intergenic variant A/G snv 0.39 3
rs6016142 1.000 0.120 20 39672165 intergenic variant C/T snv 7.8E-02 3
rs3779195
BAIAP2L1
7 98364050 intron variant T/A snv 0.16 3
rs12978500
C2CD4C
19 406934 3 prime UTR variant C/A snv 0.67 3
rs727333
DSCAM
1.000 0.080 21 40331020 intron variant C/A snv 6.6E-02 3