Disease: Cleft Palate
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
rs1038294
COL8A1
0.925 0.120 3 99784884 intron variant A/G snv 0.82 2
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
rs11582254
TMCO4
0.925 0.120 1 19691584 intron variant T/A;C snv 2
rs11774066
STK3
0.925 0.120 8 98443083 intron variant C/T snv 0.20 2
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs12375983 0.925 0.120 9 89595154 intron variant G/A snv 0.13 2
rs12681366
FSBP ; RAD54B
0.925 0.120 8 94389037 intron variant T/C snv 0.35 2
rs12944377
NTN1
0.882 0.120 17 9044391 intron variant T/C snv 0.36 3
rs1487022
VPS13B
0.925 0.120 8 99517598 intron variant G/T snv 0.17 2
rs1688766
FILIP1L ; CMSS1
0.925 0.120 3 99929006 intron variant G/A snv 0.18 2
rs1878918
NRG1
0.925 0.120 8 32476054 intron variant G/A;C snv 2
rs2073764
GNB1L
0.925 0.120 22 19811887 intron variant C/T snv 6.0E-03 2
rs2235375
IRF6
0.807 0.400 1 209792242 intron variant G/A;C;T snv 3.2E-05; 0.41; 4.3E-04 7
rs2289187
UBL7
0.925 0.120 15 74452058 intron variant C/T snv 0.24 2
rs3785888
GOSR2 ; LRRC37A2
0.925 0.120 17 46928337 intron variant C/T snv 0.51 2
rs4132699
SEMA4D
0.925 0.120 9 89421512 intron variant A/C snv 0.43 2
rs4752028
SHTN1
0.807 0.200 10 117075480 intron variant C/T snv 0.73 6
rs4791774
NTN1
0.882 0.240 17 9028802 intron variant A/C;G snv 4
rs481931
ABCA4
0.882 0.120 1 94104460 intron variant G/T snv 0.32 3
rs493760
DROSHA
0.851 0.200 5 31436933 intron variant C/T snv 0.74 5