Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4656461 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 7
rs10483727 0.851 0.040 14 60606157 upstream gene variant T/C snv 0.45 4
rs1192415 0.925 0.040 1 91611540 TF binding site variant G/A snv 0.81 4
rs4236601 0.882 0.040 7 116522675 upstream gene variant G/A snv 0.28 4
rs7081455 0.851 0.040 10 20349956 upstream gene variant G/A;T snv 4
rs747782 0.925 0.040 11 47919373 intergenic variant T/C snv 0.26 4
rs79721419 0.851 0.160 9 22200957 downstream gene variant G/A snv 7.4E-03 4
rs180040 0.882 0.120 15 97027933 intergenic variant T/C snv 0.85 3
rs3858145 0.882 0.040 10 68252081 regulatory region variant A/G snv 0.33 3
rs547984 0.882 0.040 1 237933586 intergenic variant A/C snv 0.60 3
rs17588172 0.925 0.040 7 116513961 intergenic variant T/G snv 0.35 2
rs12436579 1.000 0.040 14 60516369 intron variant C/A;G snv 1
rs4657473 1.000 0.040 1 165717914 regulatory region variant C/T snv 0.24 1
rs693421 1.000 0.040 1 237935790 downstream gene variant T/A;G snv 1
rs7098387 1.000 0.040 10 20334544 regulatory region variant A/C;T snv 0.13 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 9
rs782006965
ADAMTS10
0.925 0.040 19 8589505 missense variant C/T snv 4.0E-06 2
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs59892895
APBB2
1.000 0.040 4 40995241 intron variant T/C snv 6.6E-02 1
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs104886478
ASB10
0.925 0.040 7 151181233 synonymous variant G/A snv 5.0E-04 3.3E-04 2
rs1171063544
ASB10
1.000 0.040 7 151181278 synonymous variant G/A snv 4.0E-06 1