Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1861072
UNC80
2 209986910 intron variant T/C snv 0.34 2
rs11860711 16 81098888 upstream gene variant C/T snv 0.20 1
rs12297321 12 46715604 intron variant C/T snv 0.15 1
rs13299380 9 6078779 intergenic variant C/T snv 4.2E-02 1
rs143424675 4 72883702 intergenic variant C/A;T snv 1.4E-02 1
rs55748921 8 125480685 intron variant A/C;G;T snv 1
rs67506027 9 6657690 intron variant C/A snv 0.68 1
rs71503800 9 6102648 TF binding site variant C/T snv 2.3E-02 1
rs79064296 3 126266226 upstream gene variant G/C;T snv 2.7E-02 1
rs9514191 13 103867788 intergenic variant G/A;C snv 1
rs676996
ABO
9 133270647 intron variant G/T snv 1
rs12126607
ACADM
1 75751412 intron variant G/A snv 0.24 1
rs4646961
ACADM
1 75751484 intron variant G/A snv 0.24 1
rs3105793
ADGRV1
5 90930244 intron variant G/A snv 0.25 1
rs2280195
ALDH1A2 ; AQP9
15 58174896 intron variant G/A snv 0.37 0.40 1
rs4646705
ALDH1L1
3 126156988 intron variant G/A snv 0.52 1
rs9862438
ALDH1L1 ; ALDH1L1-AS2
3 126191538 intron variant C/T snv 0.36 1
rs156380
ARL15
5 54082620 intron variant T/A;C;G snv 1
rs9923732
C16orf46
16 81077298 intron variant A/G snv 0.11 1
rs1509820
CPS1
2 210521760 intron variant G/A snv 0.40 1
rs141015398
ENPP7P4 ; LINC02614
3 125899882 intron variant A/G snv 5.4E-03 1
rs115683961
ERBB4
2 211521195 intron variant A/G snv 3.9E-02 1
rs143119940
GLDC
9 6554781 missense variant C/A;G snv 6.4E-03; 4.1E-06 1
rs17591030
GLDC
9 6550024 intron variant C/A;T snv 1
rs10900807
IRF1-AS1 ; LINC02863
5 132421788 intron variant G/C snv 0.20 1