Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4925386
LAMA5
0.776 0.080 20 62345988 intron variant T/C snv 0.56 6
rs2070699
EDN1
0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 5
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 5
rs6691170 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 4
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 3
rs11169552
ATF1
0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 2
rs11874392
SMAD7
0.763 0.080 18 48926786 intron variant A/T snv 0.50 2
rs16969681 0.776 0.080 15 32700910 downstream gene variant C/T snv 0.11 2
rs2238126
ETV6
0.776 0.080 12 11856807 intron variant A/G snv 0.18 2
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 2
rs4813802 0.776 0.080 20 6718948 regulatory region variant T/G snv 0.28 2
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 2
rs647161
C5orf66
0.776 0.080 5 135163402 intron variant C/A snv 0.63 2
rs992157
TMBIM1 ; PNKD
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 2
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 1
rs10774214
CCND2-AS1
0.790 0.080 12 4259186 intron variant T/C snv 0.54 1
rs11064437
SPSB2
0.790 0.080 12 6872998 splice acceptor variant C/T snv 9.3E-02 1
rs1254244346
ABCA1
1.000 0.080 9 104822502 missense variant G/A snv 4.0E-06 1
rs1367374 0.790 0.080 2 153074663 intergenic variant G/C snv 0.19 1
rs142319636
MMP2
0.790 0.080 16 55504828 intron variant A/G snv 3.7E-02 1
rs1424847607
EPHA2
1.000 0.080 1 16133591 missense variant A/G snv 4.0E-06 1
rs143046984
LOC105370557 ; PCNX1
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02 1
rs16941835 0.790 0.080 16 86662114 intron variant G/C snv 0.20 1
rs17094983
LINC01500
0.776 0.080 14 58722643 intron variant G/A snv 0.12 1
rs209489
ELOVL5
0.790 0.080 6 53312880 intron variant C/A snv 0.92 1