Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10130587
BMP4
0.851 0.200 14 53952392 intron variant G/C snv 0.45 5
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 7
rs104894110
FOXE1 ; PTCSC2
0.776 0.280 9 97854108 missense variant C/T snv 8
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv 4
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
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
rs1139
ZNF385B
0.851 0.200 2 179745354 intron variant C/T snv 0.22 4
rs11466285
TGFA
0.851 0.200 2 70450307 3 prime UTR variant A/C;G snv 5
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
rs11624283 0.882 0.200 14 105124634 downstream gene variant A/G snv 0.13 3
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
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614