Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77607745 1.000 0.040 13 69001052 intergenic variant A/C snv 0.15 2
rs9972552
PGBD4
1.000 0.040 15 34104712 3 prime UTR variant A/C snv 0.99 2
rs1039197 1.000 0.040 10 4617005 intergenic variant A/C snv 0.71 1
rs10904299 1.000 0.040 10 4603975 intergenic variant A/C snv 0.21 1
rs11135349 1.000 0.040 5 165096466 intron variant A/C snv 0.61 1
rs117235991
APAF1
1.000 0.040 12 98699448 missense variant A/C snv 9.5E-03 7.8E-03 1
rs12496634
PBRM1
1.000 0.040 3 52675243 intron variant A/C snv 0.34 1
rs12923444
METTL9
1.000 0.040 16 21628389 intron variant A/C snv 0.32 1
rs1343605 1.000 0.040 13 53072913 intergenic variant A/C snv 0.63 1
rs2001144
OSTM1
1.000 0.040 6 108086458 intron variant A/C snv 0.25 1
rs2307220
PAWR
1.000 0.040 12 79592094 3 prime UTR variant A/C snv 0.36 1
rs2715148
PCLO
1.000 0.040 7 82820719 3 prime UTR variant A/C snv 0.57 1
rs346005 1.000 0.040 4 52588572 downstream gene variant A/C snv 0.47 1
rs4074723
SOX5
1.000 0.040 12 23794803 intron variant A/C snv 0.62 1
rs4687638
PBRM1
1.000 0.040 3 52617950 intron variant A/C snv 0.33 1
rs4765904
CACNA1C-AS4 ; CACNA1C
1.000 0.040 12 2223227 intron variant A/C snv 0.36 1
rs4971040 1.000 0.040 1 151394018 intergenic variant A/C snv 0.65 1
rs60545357
ATP5MG ; LOC100131626
1.000 0.040 11 118410703 intron variant A/C snv 0.20 1
rs66975207
LINC00240
1.000 0.040 6 26974367 non coding transcript exon variant A/C snv 5.7E-02 1
rs72710803 1.000 0.040 1 177458882 intron variant A/C snv 8.8E-02 1
rs72948529
ERBB4 ; MTND2P23
1.000 0.040 2 211777265 non coding transcript exon variant A/C snv 0.14 1
rs8025231 1.000 0.040 15 37356201 intergenic variant A/C snv 0.48 1
rs9386694 1.000 0.040 6 108025473 downstream gene variant A/C snv 0.45 1
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5