Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 6
rs1456079929
PGR
0.851 0.120 11 101042001 missense variant C/A snv 8.0E-06 5
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 5
rs755378873
SLC13A5
0.851 0.120 17 6694197 missense variant C/A;T snv 4.0E-06 5
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 4
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 4
rs192876988
LOC105377300
0.851 0.120 4 79376097 intergenic variant T/C snv 1.6E-02 4
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 4
rs67164370
RASSF2
0.851 0.120 20 4787830 intron variant -/AGGGACT ins 4
rs10260419
THSD7A
0.882 0.120 7 11524758 intron variant C/G snv 0.26 3
rs1649942
NRG3
0.925 0.120 10 82191935 intron variant G/A;C snv 3
rs2252673
INSR
0.882 0.120 19 7150407 intron variant C/G snv 0.75 3
rs56318008
LOC105376845 ; WNT4
0.925 0.120 1 22143914 5 prime UTR variant C/T snv 0.13 3
rs74917072
UBE2F ; UBE2F-SCLY
0.882 0.120 2 238022053 intron variant G/A;T snv 3
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 3
rs7748275 0.882 0.120 6 3580855 downstream gene variant T/A snv 8.2E-02 3
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 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