Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1037189404
MUC1
0.776 0.280 1 155187519 missense variant C/T snv 8
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs766333007
MUC1
0.776 0.280 1 155192274 missense variant C/T snv 7.0E-06 8
rs9582036
FLT1
0.776 0.280 13 28311271 intron variant C/A snv 0.59 8
rs2195239
LINC02456 ; IGF1
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28 7
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs3790843
NR5A2
0.827 0.160 1 200041696 intron variant C/T snv 0.29 7
rs587778883
MLH1
0.807 0.200 3 37025648 frameshift variant A/- del 7
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 6
rs11571836
BRCA2
0.827 0.200 13 32399302 3 prime UTR variant A/G;T snv 6
rs1561927
LINC00824
0.807 0.280 8 128555832 intron variant C/T snv 0.65 6
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 6
rs4668123
LRP2
0.851 0.280 2 169196995 missense variant C/A;G;T snv 6
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 5
rs2239186
VDR
0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 5
rs372883
BACH1
0.827 0.360 21 29345416 3 prime UTR variant T/C snv 0.53 5
rs587779067
MSH2
0.882 0.200 2 47416399 missense variant C/G;T snv 5
rs7675998 0.827 0.360 4 163086668 intergenic variant A/G;T snv 5
rs80358683
BRCA2
0.851 0.120 13 32338880 stop gained C/T snv 5
rs9502893 0.827 0.120 6 1339954 intergenic variant C/G;T snv 5
rs1176026649
CBR4 ; PALLD
0.851 0.120 4 168921582 missense variant C/T snv 7.2E-06 4
rs2941471
HNF4G
0.851 0.240 8 75558169 intron variant G/A snv 0.65 4
rs3790844
NR5A2
0.882 0.200 1 200038304 intron variant A/C;G snv 4
rs4759313
HOTAIR
0.851 0.120 12 53965290 intron variant T/A snv 0.51 4