Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 1
rs497309
CYP21A2 ; C2
0.882 0.240 6 31924707 intron variant A/C;G snv 1
rs74617384
LPA
0.925 0.080 6 160576086 intron variant A/G;T snv 1
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 1
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 1
rs10818684 1.000 0.040 9 122407651 intron variant C/T snv 0.62 2
rs11071657 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 2
rs1206634 1.000 0.040 X 96302380 intron variant T/A;G snv 2
rs1260236 1.000 0.040 9 6023030 intergenic variant A/G snv 2
rs12910524 1.000 0.040 15 101262360 intergenic variant T/A;C snv 2
rs1543654 1.000 0.040 21 34426752 upstream gene variant T/C snv 2
rs181914932 1.000 0.040 20 45932640 non coding transcript exon variant T/C snv 1.6E-02 2
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 2
rs2863389 1.000 0.040 3 166431104 intergenic variant C/T snv 0.17 2
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 2
rs4900384 0.882 0.160 14 98032614 intergenic variant A/G snv 0.40 2
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 2
rs57922 1.000 0.040 5 74282114 intron variant C/T snv 0.40 2
rs675209 0.882 0.160 6 7101851 intergenic variant T/C snv 0.64 2
rs7172432 0.925 0.080 15 62104190 intergenic variant A/G snv 0.51 2
rs148529020
ABCC8
1.000 0.040 11 17460613 missense variant C/T snv 1.2E-05 1.4E-05 2
rs28938469
ABCC8
0.925 0.160 11 17395659 missense variant G/A snv 2
rs756823374
ABCC8
1.000 0.040 11 17463515 missense variant G/A snv 1.4E-05 2
rs2199936
ABCG2
0.882 0.160 4 88124179 intron variant A/G;T snv 0.88 2
rs735949
ACSL1
0.925 0.080 4 184795078 intron variant T/C snv 0.10 2