Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801198
TCN2
0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs2235371
IRF6
0.752 0.360 1 209790735 missense variant C/T snv 8.7E-02 3.9E-02 11
rs147680216
WNT10A
0.742 0.160 2 218890244 missense variant G/A snv 2.1E-03 6.9E-04 11
rs199469464
SRCAP
0.807 0.200 16 30737370 stop gained C/T snv 8
rs12543318 0.882 0.120 8 87856112 intergenic variant C/A snv 0.68 4
rs4920037
CBS
0.851 0.080 21 43061781 intron variant G/A snv 4
rs6072081
LOC102724968
0.851 0.120 20 40632414 intergenic variant A/G snv 0.49 4
rs11841646 0.882 0.120 13 80105167 intergenic variant T/A;G snv 0.42 3
rs6029258 0.882 0.120 20 40656135 intergenic variant G/A snv 0.58 3
rs7566780 0.882 0.120 2 16548089 intron variant A/C;G snv 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
rs12944377
NTN1
0.882 0.120 17 9044391 intron variant T/C snv 0.36 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
rs10886040
SHTN1
0.882 0.120 10 117086783 intron variant C/G snv 0.20 3
rs76479869
TP63
0.882 0.120 3 189835583 intron variant C/T snv 4.3E-02 3
rs3789432
ABCA4
0.925 0.080 1 94109752 intron variant T/C snv 0.33 2
rs1109430 1.000 1 209819156 intergenic variant G/A snv 3.9E-02 1
rs12070337 1.000 1 209818782 intergenic variant G/A snv 0.21 1
rs12347191 1.000 9 97857437 upstream gene variant C/T snv 0.63 1
rs17242358
CCDC26 ; LINC00976
1.000 8 128952627 intron variant G/A snv 0.14 1