Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 8
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 5
rs2070803
TRIM46
0.925 0.080 1 155185239 intron variant G/A snv 0.55 5
rs4971100
TRIM46
0.925 0.120 1 155183255 intron variant G/A snv 0.39 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs11264341
TRIM46
0.925 0.120 1 155179017 intron variant C/T snv 0.40 4
rs10910845 0.925 0.120 1 145711946 upstream gene variant T/G snv 0.44 3
rs12123298
RNF115
0.925 0.120 1 145744615 3 prime UTR variant G/A;C snv 0.27 3
rs12129861
PDZK1
0.925 0.120 1 145709377 upstream gene variant C/T snv 0.43 3
rs1471633 0.925 0.120 1 145711327 upstream gene variant T/G snv 0.43 3
rs4970988 0.925 0.120 1 150977586 upstream gene variant G/A snv 0.30 3
rs7555340
ZMYM6
0.925 0.120 1 35015950 intron variant T/C snv 6.2E-03 3
rs9728619
PDZK1
0.925 0.120 1 145698627 intron variant A/G snv 0.51 3
rs12134456
GON4L
1 155752715 intron variant C/G snv 0.26 2
rs12135191 1 236307434 regulatory region variant C/G;T snv 2
rs139428292
RBM8A ; LIX1L-AS1
1.000 0.120 1 145927447 5 prime UTR variant C/A;T snv 4.2E-06; 1.8E-02 2
rs1797052
PDZK1
1 145707383 5 prime UTR variant A/G;T snv 2
rs10803394
AGMAT ; DNAJC16
1 15582985 intron variant G/A;C snv 1
rs10890263
PTPRF
1 43595361 intron variant T/C snv 0.20 1
rs10908521
NTRK1 ; INSRR
1 156843858 intron variant T/C snv 0.31 1
rs11204701
GOLPH3L
1 150689703 intron variant A/T snv 0.17 1
rs12037861
HLX-AS1
1 220864835 intron variant A/T snv 0.28 1
rs141990161 1 119400902 intergenic variant T/A;C;G snv 1