Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008257 0.925 0.040 4 94435177 intergenic variant G/A snv 0.63 2
rs10035291
SSBP2
1.000 0.040 5 81500549 intron variant T/C snv 0.46 1
rs10051667
GABRB2
0.925 0.080 5 161471322 intron variant T/C snv 0.12 2
rs10058613
KDM3B
0.925 0.040 5 138358306 intron variant C/A;G;T snv 2
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1012053
DGKH
1.000 0.040 13 42079301 intron variant C/A snv 0.85 1
rs10134944
SLC35F4
1.000 0.040 14 57652478 intron variant C/T snv 0.13 1
rs10168049 1.000 0.040 2 121320830 intergenic variant A/G snv 0.16 1
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 3
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs1033656351
P2RX4
0.827 0.160 12 121232997 missense variant G/A snv 1.6E-05 2.8E-05 7
rs1034936
CACNA1C
0.882 0.080 12 2551994 intron variant C/T snv 0.61 3
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042779
ITIH1
0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 4
rs10455979
RPS6KA2
1.000 0.040 6 166581772 intron variant C/A;G;T snv 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10457441 1.000 0.040 6 98124244 intron variant T/A;C snv 2
rs10459221 1.000 0.040 12 49073211 upstream gene variant C/A;G snv 1
rs10462020
PER3
0.925 0.160 1 7820623 missense variant T/G snv 0.17 0.16 2
rs10488140
EGFR
1.000 0.040 7 55070695 intron variant C/T snv 0.26 1
rs10489167
NFYC
1.000 0.040 1 40710794 intron variant G/A snv 0.13 1
rs10489744
RXRG
0.925 0.040 1 165411386 intron variant G/A snv 0.55 2
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42