Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv 4
rs12543318 0.882 0.120 8 87856112 intergenic variant C/A snv 0.68 4
rs227731 0.882 0.120 17 56695877 intergenic variant T/A;G snv 4
rs6072081
LOC102724968
0.851 0.120 20 40632414 intergenic variant A/G snv 0.49 4
rs7078160
SHTN1
0.851 0.120 10 117068049 intron variant G/A snv 0.19 4
rs10886040
SHTN1
0.882 0.120 10 117086783 intron variant C/G snv 0.20 3
rs11841646 0.882 0.120 13 80105167 intergenic variant T/A;G snv 0.42 3
rs12944377
NTN1
0.882 0.120 17 9044391 intron variant T/C snv 0.36 3
rs13317
FGFR1
0.882 0.120 8 38411996 3 prime UTR variant T/C snv 0.23 3
rs481931
ABCA4
0.882 0.120 1 94104460 intron variant G/T snv 0.32 3
rs6029258 0.882 0.120 20 40656135 intergenic variant G/A snv 0.58 3
rs66515264
ABCA4
0.882 0.120 1 94092554 intron variant G/A;T snv 3
rs72728734
CCDC26
0.882 0.120 8 128921474 intron variant A/G snv 0.13 3
rs7552
CYRIA
0.882 0.120 2 16552660 splice region variant A/G snv 0.44 3
rs7566780 0.882 0.120 2 16548089 intron variant A/C;G snv 3
rs76479869
TP63
0.882 0.120 3 189835583 intron variant C/T snv 4.3E-02 3
rs9439713
PAX7
0.882 0.120 1 18646282 intron variant G/A snv 0.31 3
rs9439714
PAX7
0.882 0.120 1 18649995 intron variant T/C snv 0.28 3
rs10133673
SLC25A21
0.925 0.120 14 37068147 intron variant T/C snv 2.8E-02 2
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
rs10808812
LOC107986952 ; ZFHX4-AS1
0.925 0.120 8 76593073 intron variant T/C snv 0.23 2
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