Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2781667
MED23 ; ARG1
0.851 0.080 6 131574004 3 prime UTR variant C/T snv 0.45 4
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 4
rs41508050
HIF1A-AS3 ; HIF1A
0.882 0.080 14 61738090 missense variant C/T snv 3.8E-03 4.0E-03 4
rs4986970
LCAT
0.925 0.080 16 67942417 missense variant A/C;T snv 4.0E-06; 1.7E-02 4
rs6725887
WDR12
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 4
rs8089
LOC101929523 ; THBS2
0.851 0.080 6 169217631 splice region variant A/C snv 0.22 4
rs9319428
FLT1
0.925 0.080 13 28399484 intron variant G/A snv 0.30 4
rs9369640
PHACTR1
0.851 0.080 6 12901209 intron variant C/A;G snv 4
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 4
rs11572325
CYP2J2
0.925 0.080 1 59896030 intron variant A/T snv 0.12 3
rs1169286
HNF1A
1.000 0.080 12 120981253 intron variant T/C snv 0.39 3
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs121918529
MEF2A
0.882 0.080 15 99690400 missense variant C/T snv 6.1E-04 6.5E-04 3
rs12632110
SEMA3F
1.000 0.080 3 50186792 intron variant A/G snv 0.63 0.62 3
rs197922
GOSR2 ; LRRC37A2
0.925 0.080 17 46931204 missense variant G/A snv 0.35 0.33 3
rs200340021
C12orf60 ; MGP
0.925 0.080 12 14882204 missense variant C/T snv 7.0E-06 3
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs2246833
LIPA
0.882 0.080 10 89246097 intron variant C/T snv 0.38 3
rs2251393
MARCHF10
1.000 0.080 17 62701571 3 prime UTR variant G/A;C snv 0.85; 4.9E-05 3
rs2301339
CDCA3 ; GNB3
1.000 0.080 12 6845460 3 prime UTR variant G/A;T snv 3
rs2505083
JCAD
0.882 0.080 10 30046193 intron variant T/C snv 0.33 3
rs2781668
ARG1 ; MED23
1.000 0.080 6 131576138 intron variant C/T snv 0.16 3
rs28451064 0.925 0.080 21 34221526 intron variant G/A snv 9.2E-02 3
rs3744700
CXCL16
0.882 0.080 17 4734715 intron variant T/G snv 0.66 3
rs532436
ABO
1.000 0.080 9 133274414 intron variant A/G;T snv 3