Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113577745
GRHL1
1.000 0.080 2 9995553 intron variant C/G snv 8.8E-02 1
rs148972953
LAMTOR3
0.925 0.080 4 99881589 3 prime UTR variant A/G snv 8.8E-03 3
rs2273697
ABCC2
0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 11
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs2242480
CYP3A4
0.882 0.120 7 99763843 intron variant C/T snv 0.22 0.32 5
rs4986910
CYP3A4
0.925 0.080 7 99760901 missense variant A/G snv 5.2E-03 5.1E-03 3
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 9
rs11298677
COL8A1
1.000 0.080 3 99682866 intron variant G/- delins 0.60 1
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs200764640
ZSCAN25 ; CYP3A5
0.925 0.080 7 99666641 missense variant T/C snv 4.0E-06 2
rs10273424
TMEM225B
0.925 0.080 7 99598450 intron variant T/A snv 0.13 3
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs1045012
ARPC1B
0.925 0.080 7 99386731 missense variant G/C snv 5.6E-02 7.8E-02 2
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs334348
TGFBR1
0.851 0.160 9 99150189 3 prime UTR variant A/G;T snv 5
rs1178346731
TGFBR1
0.925 0.080 9 99144783 missense variant A/G snv 4.0E-06 2
rs531564
LINC00599 ; MIR124-1
0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs2016347
IGF1R
0.790 0.160 15 98960571 3 prime UTR variant G/A;T snv 9
rs12916884
IGF1R
0.925 0.080 15 98944659 intron variant G/T snv 0.25 2
rs11635251
IGF1R
0.925 0.080 15 98937442 intron variant A/G snv 0.17 2
rs12439557
IGF1R
0.925 0.080 15 98771553 intron variant T/C snv 0.74 2
rs8032477
IGF1R
0.851 0.200 15 98711325 intron variant C/A;T snv 4
rs3735684
C7orf50 ; CYP2W1
0.851 0.120 7 985219 missense variant G/A snv 6.8E-02 7.3E-02 4
rs79518236
BAIAP2L1
1.000 0.080 7 98397243 intron variant CT/- delins 0.24 1