Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1127313
ADAR ; CHRNB2
1.000 0.120 1 154583949 3 prime UTR variant G/A snv 0.41 1
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 5
rs1649942
NRG3
0.925 0.120 10 82191935 intron variant G/A;C snv 3
rs56318008
LOC105376845 ; WNT4
0.925 0.120 1 22143914 5 prime UTR variant C/T snv 0.13 3
rs10017134
UGT2A2 ; UGT2A1
0.925 0.120 4 69591303 intron variant T/C snv 0.75 2
rs1002076
KIF1B
0.925 0.120 1 10378834 3 prime UTR variant G/A snv 0.33 2
rs1017134 0.925 0.120 7 35307237 intergenic variant G/A snv 0.47 2
rs1057156
RUVBL1
0.925 0.120 3 128081228 3 prime UTR variant A/G snv 0.22 0.23 2
rs10788679
ARHGEF10L
0.925 0.120 1 17590467 intron variant A/G snv 0.59 2
rs11175194
SRGAP1
0.925 0.120 12 63871057 intron variant G/A snv 0.15 2
rs114972508
EGFR ; LOC105375284
0.925 0.120 7 55020815 intron variant T/C snv 1.4E-02 2
rs11696662
PLCG1
0.925 0.120 20 41161795 intron variant C/T snv 4.4E-02 2
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