Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4752028
SHTN1
0.807 0.200 10 117075480 intron variant C/T snv 0.73 6
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
rs6838801
SHROOM3 ; LOC105377290
0.925 0.120 4 76628406 intron variant G/T snv 0.29 2
rs2006771
SFI1
0.925 0.120 22 31602626 missense variant G/A snv 0.41 0.44 2
rs4132699
SEMA4D
0.925 0.120 9 89421512 intron variant A/C snv 0.43 2
rs2239907
SARM1 ; SLC46A1
0.851 0.200 17 28398728 3 prime UTR variant T/C snv 0.53 5
rs6126344
SALL4
0.925 0.120 20 51790963 missense variant A/C;T snv 0.35; 8.0E-06 2
rs705704
RPS26 ; LOC105369780
0.882 0.240 12 56041628 non coding transcript exon variant G/A snv 0.26 4
rs3905385
ROR2
0.882 0.200 9 91906451 intron variant T/C snv 0.23 3
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv 4
rs12175475
PRKN
1.000 0.120 6 162250424 intron variant A/T snv 2.1E-02 1
rs587777450
PIEZO2
0.790 0.320 18 10671729 missense variant C/T snv 9
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
rs742071
PAX7
0.925 0.120 1 18653380 intron variant G/T snv 0.39 2
rs11597348
OPALIN
1.000 0.120 10 96354046 intron variant A/T snv 7.9E-02 1
rs4791774
NTN1
0.882 0.240 17 9028802 intron variant A/C;G snv 4
rs12944377
NTN1
0.882 0.120 17 9044391 intron variant T/C snv 0.36 3
rs9911652
NTN1
0.925 0.120 17 9039746 intron variant C/T snv 0.16 2
rs1878918
NRG1
0.925 0.120 8 32476054 intron variant G/A;C snv 2
rs1474322770
NKX2-1 ; NKX2-1-AS1 ; SFTA3
0.827 0.240 14 36519251 missense variant G/A snv 5
rs11066150
NAA25
0.925 0.120 12 112080999 intron variant G/A snv 1.3E-02 2
rs2269529
MYH9 ; MIR6819
0.851 0.200 22 36288308 missense variant T/C snv 0.26 0.18 5