Disease: Cleft Palate
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs55658222
LINC00976 ; CCDC26
0.925 0.120 8 128963890 intron variant G/A snv 0.14 2
rs560426
ABCA4
0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs6495117
LOC102723750 ; CLK3
0.925 0.120 15 74607159 intron variant T/C snv 0.26 2
rs66515264
ABCA4
0.882 0.120 1 94092554 intron variant G/A;T snv 3
rs6740960
C2orf91
0.925 0.120 2 41954539 intron variant A/T snv 0.61 2
rs68092024
CMSS1 ; FILIP1L
0.925 0.120 3 99972678 intron variant C/T snv 0.68 2
rs6838801
SHROOM3 ; LOC105377290
0.925 0.120 4 76628406 intron variant G/T snv 0.29 2
rs7017252
CCDC26
0.925 0.120 8 128938598 intron variant C/T snv 0.32 2
rs7078160
SHTN1
0.851 0.120 10 117068049 intron variant G/A snv 0.19 4
rs7148069 0.925 0.120 14 51372927 intron variant C/T snv 0.32 2
rs72728734
CCDC26
0.882 0.120 8 128921474 intron variant A/G snv 0.13 3
rs742071
PAX7
0.925 0.120 1 18653380 intron variant G/T snv 0.39 2
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
rs7692299
LINC01091
0.925 0.120 4 123789429 intron variant C/T snv 0.15 2
rs78212183
DEPDC5
0.925 0.120 22 31817998 intron variant T/C snv 1.1E-02 2
rs7871395 0.925 0.120 9 89594672 intron variant C/T snv 0.24 2
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
rs9545308 0.925 0.120 13 80065270 intron variant G/T snv 0.21 2
rs9911652
NTN1
0.925 0.120 17 9039746 intron variant C/T snv 0.16 2
rs112800917
LOC105373887
0.925 0.120 2 219743055 intergenic variant CACAGAAT/- delins 0.54 2
rs11841646 0.882 0.120 13 80105167 intergenic variant T/A;G snv 0.42 3
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs1243572 0.925 0.120 14 94913162 intergenic variant T/C snv 0.78 2