Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 11
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 8
rs6020712
CTNNBL1
1.000 0.080 20 37758210 intron variant G/A snv 0.12 4
rs11237982 1.000 0.080 11 79730650 intergenic variant T/C snv 0.18 2
rs117905930 1.000 0.080 9 88973603 intron variant C/A;T snv 2
rs147906088 1.000 0.080 7 54496119 intergenic variant C/A;T snv 2
rs72639058
KAZN
1.000 0.080 1 13913797 intron variant C/A;T snv 2
rs6479525
LINC01508
1.000 0.080 9 90331096 intron variant G/A snv 0.44 2
rs62187521
RSPO4
1.000 0.080 20 959154 3 prime UTR variant C/T snv 4.8E-03 2
rs56214552
TRIQK
1.000 0.080 8 93011994 intron variant T/G snv 0.24 2
rs2976464
ZNF250
1.000 0.040 8 144902955 upstream gene variant A/G snv 0.46 2
rs10058621 5 51259335 intergenic variant T/C snv 6.0E-02 1
rs11074779 16 26440122 intergenic variant T/C snv 0.16 1
rs12436690 14 97119552 intron variant G/A snv 0.12 1
rs12990252 2 35861457 intergenic variant G/C snv 0.18 1
rs13166268 5 121024223 intergenic variant C/G snv 9.2E-02 1
rs140454225 16 1003856 upstream gene variant T/C;G snv 1
rs1449587 13 48839332 regulatory region variant C/T snv 0.31 1
rs145471199 7 9407441 intergenic variant A/G;T snv 1
rs150900094 15 87284961 intergenic variant A/C snv 2.9E-02 1
rs35551159 12 60075450 intergenic variant C/A;T snv 1
rs4762194 12 97789941 intergenic variant G/A snv 0.20 1