Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10133673
SLC25A21
0.925 0.120 14 37068147 intron variant T/C snv 2.8E-02 2
rs10242177 1.000 0.120 7 156369656 intergenic variant C/A;T snv 1
rs1038294
COL8A1
0.925 0.120 3 99784884 intron variant A/G snv 0.82 2
rs10462065 0.925 0.120 5 44068744 upstream gene variant C/A snv 8.3E-02 2
rs104893810
TGFBR2
0.790 0.360 3 30691477 missense variant C/T snv 3
rs104894110
FOXE1 ; PTCSC2
0.776 0.280 9 97854108 missense variant C/T snv 1
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv 4
rs10808812
LOC107986952 ; ZFHX4-AS1
0.925 0.120 8 76593073 intron variant T/C snv 0.23 2
rs10886040
SHTN1
0.882 0.120 10 117086783 intron variant C/G snv 0.20 3
rs11066150
NAA25
0.925 0.120 12 112080999 intron variant G/A snv 1.3E-02 2
rs11072494
ARID3B
0.925 0.120 15 74596822 3 prime UTR variant C/G;T snv 2
rs112800917
LOC105373887
0.925 0.120 2 219743055 intergenic variant CACAGAAT/- delins 0.54 2
rs113691307
LOC102724542
1.000 0.120 2 81801266 intergenic variant C/T snv 6.1E-02 1
rs11582254
TMCO4
0.925 0.120 1 19691584 intron variant T/A;C snv 2
rs11597348
OPALIN
1.000 0.120 10 96354046 intron variant A/T snv 7.9E-02 1
rs117496742
YAP1
1.000 0.120 11 102208982 intron variant G/A;T snv 1.3E-02 1
rs11774066
STK3
0.925 0.120 8 98443083 intron variant C/T snv 0.20 2
rs11841646 0.882 0.120 13 80105167 intergenic variant T/A;G snv 0.42 3
rs12175475
PRKN
1.000 0.120 6 162250424 intron variant A/T snv 2.1E-02 1
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 2
rs12375983 0.925 0.120 9 89595154 intron variant G/A snv 0.13 2
rs1243572 0.925 0.120 14 94913162 intergenic variant T/C snv 0.78 2
rs12543318 0.882 0.120 8 87856112 intergenic variant C/A snv 0.68 3
rs12681366
FSBP ; RAD54B
0.925 0.120 8 94389037 intron variant T/C snv 0.35 2