Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 15
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 10
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 8
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 3
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 2
rs16969681 0.776 0.080 15 32700910 downstream gene variant C/T snv 0.11 2
rs4813802 0.776 0.080 20 6718948 regulatory region variant T/G snv 0.28 2
rs10957057 1.000 0.080 8 58487781 downstream gene variant C/T snv 0.12 1
rs11022858 1.000 0.080 11 13505086 intergenic variant T/A;C snv 1
rs13251096 1.000 0.080 8 58505225 downstream gene variant A/G snv 0.53 1
rs846672 1.000 0.080 7 122990126 downstream gene variant A/C;T snv 1
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 60
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 93
rs201745983
ALDH2
0.752 0.200 12 111783219 missense variant G/A snv 6.8E-05 7.7E-05 14
rs1126667
ALOX12 ; ALOX12-AS1
0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
rs2287939
AMACR ; C1QTNF3-AMACR
0.851 0.160 5 33998778 missense variant A/C;G snv 1.6E-05; 0.70 4
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 36
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 16
rs770649674
APC
0.807 0.120 5 112827177 missense variant A/G snv 4.0E-06 7.0E-06 6
rs762117133
APC
1.000 0.080 5 112801324 missense variant C/A;T snv 2.4E-05 3
rs3733890
BHMT ; DMGDH
0.708 0.480 5 79126136 missense variant G/A snv 0.30 0.28 16
rs3087967
C11orf53
0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 1