Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1192691 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 2
rs1413299
COL15A1
0.925 0.120 9 98998959 intron variant G/A;T snv 2
rs142091544 0.925 0.120 5 168286995 upstream gene variant C/T snv 2.1E-02 2
rs146314922
NLRP2
0.925 0.120 19 54982828 missense variant A/G snv 2
rs149652370
RUVBL1
0.925 0.120 3 128084115 non coding transcript exon variant A/G snv 1.3E-04 2
rs1596797
MUC16
0.925 0.120 19 8977341 missense variant T/A;C;G snv 2.0E-05; 4.0E-06; 0.74 2
rs17106154
RAD51B
0.925 0.120 14 68694457 non coding transcript exon variant T/C snv 7.8E-02 2
rs17250239
TRAF2
0.925 0.120 9 136902178 non coding transcript exon variant G/A snv 7.2E-02 2
rs17329882
SYNPO2
0.925 0.120 4 119028805 intron variant A/C;T snv 2
rs17427875
HOXA11 ; HOXA11-AS
0.925 0.120 7 27185939 non coding transcript exon variant A/T snv 0.15 2
rs17507066
CHEK2
0.925 0.120 22 28696732 intron variant C/T snv 7.0E-02 2
rs17702471
GPC6
0.925 0.120 13 93224864 upstream gene variant A/G snv 0.16 2
rs1955513
AKAP6
0.925 0.120 14 32706736 intron variant T/G snv 0.11 2
rs1983383
CAPN13
0.925 0.120 2 30754766 intron variant C/A snv 0.39 2
rs2190503
GRB10
0.925 0.120 7 50674920 intron variant A/G;T snv 2
rs2256787
ARHGEF10L
0.925 0.120 1 17566321 intron variant A/C snv 0.93 2
rs237028
TAB2
0.925 0.120 6 149397514 intron variant C/T snv 0.58 2
rs2803073
PRKN
0.925 0.120 6 162541796 intron variant G/A snv 0.74 2
rs3087714
SULF1
0.925 0.120 8 69660769 3 prime UTR variant G/A snv 0.30 2
rs372150314
SHMT1
0.925 0.120 17 18347596 missense variant C/A;T snv 4.0E-06 2
rs3745546
INSR
0.925 0.120 19 7211805 intron variant G/A;C snv 2
rs3769827
CASP8
0.925 0.120 2 201237962 intron variant A/G snv 0.42 2
rs3820282
LOC105376845 ; WNT4
0.925 0.120 1 22141722 intron variant C/T snv 0.13 2
rs41324349
CARD11
0.925 0.120 7 2907529 intron variant G/A;C;T snv 2
rs4286604 0.925 0.120 4 69576447 intron variant A/G snv 0.76 2