Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10006327
SLC9B1
1.000 0.080 4 102969823 intron variant T/A;C snv 1
rs10027347
ARHGAP10
1.000 0.080 4 148025539 intron variant G/T snv 7.7E-02 1
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs10163755
DSG4 ; DSG1-AS1
0.827 0.200 18 31405413 intron variant G/A snv 0.74 6
rs10165883 1.000 0.080 2 69889883 upstream gene variant C/T snv 0.59 1
rs10213171
ARHGAP10
1.000 0.080 4 148016386 intron variant C/G snv 0.12 1
rs10240738
AOC1 ; LOC105375567
1.000 0.080 7 150847046 intron variant C/T snv 0.59 1
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10428132
SCN10A
0.925 0.120 3 38736063 intron variant T/G snv 0.67 2
rs1044258
ARMH3 ; LOC107984029
1.000 0.080 10 101845957 3 prime UTR variant T/C snv 0.26 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10458660
LRMDA
1.000 0.080 10 76176818 intron variant A/G snv 0.19 1
rs10465885
LOC102723321 ; GJA5
0.882 0.080 1 147760632 intron variant T/A;C snv 4
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 4
rs10479177
FAM13B
1.000 0.080 5 138052751 upstream gene variant A/G snv 0.30 1
rs104893904
NKX2-5
0.807 0.160 5 173235023 missense variant C/G snv 1.1E-03 7.1E-04 6
rs104894021
KCNH2
0.851 0.120 7 150951629 missense variant G/C;T snv 5
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv 6
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14 3
rs10504554
LY96
1.000 0.080 8 74007478 intron variant T/C snv 0.27 1
rs10520260
HAND2
1.000 0.080 4 173526198 3 prime UTR variant A/G snv 0.27 1
rs10741807
NAV2
1.000 0.080 11 19989899 intron variant T/A;C snv 1
rs10749053
RBM20
1.000 0.080 10 110816937 intron variant T/A;C snv 1
rs10753933
PPFIA4
1.000 0.080 1 203057086 intron variant T/G snv 0.47 1
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44