Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467
HIF1A ; HIF1A-AS3
0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs763538721
HIF1A-AS3 ; HIF1A
0.807 0.160 14 61740897 missense variant T/A snv 4.0E-06 8
rs1430452530
HIF1A-AS3 ; HIF1A
0.851 0.160 14 61721518 missense variant A/G snv 4.0E-06 5
rs41508050
HIF1A-AS3 ; HIF1A
0.882 0.080 14 61738090 missense variant C/T snv 3.8E-03 4.0E-03 4
rs142179458
HIF1A-AS3 ; HIF1A
0.925 0.080 14 61736905 missense variant G/A snv 2.2E-03 9.1E-04 2
rs2301113
HIF1A-AS3 ; HIF1A
0.925 0.120 14 61739830 intron variant C/A snv 0.60 2
rs574603732
HIF1A-AS3 ; HIF1A
0.925 0.080 14 61740832 missense variant G/A;C snv 1.6E-05; 4.0E-06 2
rs1957757
HIF1A-AS3 ; HIF1A
1.000 0.080 14 61730230 intron variant T/C snv 0.74 1
rs7156573
HIF1A-AS3 ; HIF1A
14 61711103 intron variant G/A snv 0.94 1
rs748620045
HIF1A-AS3 ; HIF1A
1.000 0.040 14 61738213 missense variant C/T snv 4.0E-06 7.0E-06 1
rs779702949
HIF1A-AS3 ; HIF1A
14 61740887 missense variant A/C snv 4.0E-06 1
rs10138032
HIF1A ; HIF1A-AS3
14 61717464 intron variant A/G snv 8.8E-02 1
rs10873142
HIF1A ; HIF1A-AS3
1.000 0.040 14 61736744 intron variant C/T snv 0.67 1