Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72928364
ABI3BP
1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs4149310
ABCA1
9 104826853 intron variant A/T snv 0.34 3
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs59490629
PDSS2
1.000 0.080 6 107256268 intron variant G/A snv 8.5E-02 2
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs3809346
COL4A1 ; COL4A2
1.000 0.080 13 110308596 intron variant G/A;C snv 2
rs3798722
ELOVL2
6 11040190 intron variant A/G snv 0.39 2
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs9641609 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs59811240
MTSS1
1.000 0.080 8 124709787 intron variant C/A snv 1.3E-02 2
rs75629841
MTSS1
1.000 0.080 8 124714135 intron variant G/A;T snv 2
rs6898559
ALDH7A1
1.000 0.080 5 126557237 intron variant G/A snv 0.66 2
rs10807323
PHACTR1
6 12794799 intron variant G/A snv 0.34 1
rs2026458
PHACTR1
0.882 0.080 6 12825642 intron variant C/T snv 0.34 6
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs4711863
PHACTR1
6 12915185 intron variant G/C snv 0.29 1
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs113533135
LRP1B
1.000 0.080 2 140268867 intron variant T/C snv 2.0E-02 2
rs1532002
LRP1B
1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs7804216
ACTR3C
1.000 0.080 7 149941248 intergenic variant C/G snv 0.24 2
rs9384331
LOC105378054
1.000 0.080 6 150279905 intergenic variant T/C snv 0.12 2
rs4272321
PTPRN2
1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 2