Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2235375
IRF6
0.807 0.400 1 209792242 intron variant G/A;C;T snv 3.2E-05; 0.41; 4.3E-04 7
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs4752028
SHTN1
0.807 0.200 10 117075480 intron variant C/T snv 0.73 6
rs10130587
BMP4
0.851 0.200 14 53952392 intron variant G/C snv 0.45 5
rs2326398
CRISPLD2
0.827 0.200 16 84869111 intron variant A/G snv 0.37 5
rs493760
DROSHA
0.851 0.200 5 31436933 intron variant C/T snv 0.74 5
rs560426
ABCA4
0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv 4
rs1139
ZNF385B
0.851 0.200 2 179745354 intron variant C/T snv 0.22 4
rs197204
MCUB
0.851 0.200 4 109576918 intron variant C/G snv 0.52 4
rs4791774
NTN1
0.882 0.240 17 9028802 intron variant A/C;G snv 4
rs6757845
ZNF385B
0.851 0.200 2 179449268 intron variant T/C snv 0.66 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
rs12944377
NTN1
0.882 0.120 17 9044391 intron variant T/C snv 0.36 3
rs2076056
JARID2
0.882 0.200 6 15487551 intron variant C/A;G;T snv 0.24 3
rs2237138
JARID2
0.882 0.200 6 15463164 intron variant T/C snv 0.22 3
rs227493 0.882 0.200 6 165071698 intron variant A/T snv 1.7E-02 3
rs3905385
ROR2
0.882 0.200 9 91906451 intron variant T/C snv 0.23 3
rs481931
ABCA4
0.882 0.120 1 94104460 intron variant G/T snv 0.32 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
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