Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11265269 1.000 0.080 1 159758337 upstream gene variant T/C snv 0.26 1
rs1010419
AGBL1
1.000 0.080 15 86992870 intron variant A/G snv 0.55 1
rs2701405
AGBL1
1.000 0.080 15 86996687 intron variant C/A snv 0.51 1
rs10152333
AGBL1-AS1 ; AGBL1
1.000 0.080 15 86311128 intron variant T/C snv 0.57 1
rs72791417
CTNNA3
1.000 0.080 10 65983896 intron variant A/T snv 0.11 1
rs1457319153
DAG1
1.000 0.080 3 49531991 missense variant A/C snv 4.0E-06 1
rs5927969
DMD
1.000 0.080 X 32331318 intron variant T/A;G snv 1
rs7887541
DMD
1.000 0.080 X 32053387 intron variant T/C snv 0.29 1
rs1042606
DUSP5
1.000 0.080 10 110510917 3 prime UTR variant A/C snv 0.64 1
rs3793892
DUSP5
1.000 0.080 10 110505377 intron variant G/T snv 0.65 1
rs3771150
IL18RAP
1.000 0.080 2 102444391 intron variant G/A snv 0.22 1
rs4829242
IL1RAPL1
1.000 0.080 X 29613413 intron variant C/T snv 0.35 1
rs6526874
IL1RAPL1
1.000 0.080 X 29508403 intron variant T/A;C;G snv 1
rs1440306
LOC107986306
1.000 0.080 4 116954105 upstream gene variant T/A;G snv 1
rs2664349
MMP16
1.000 0.080 8 88077054 intron variant G/A snv 0.65 1
rs2664352
MMP16
1.000 0.080 8 88081070 intron variant T/C snv 0.50 1
rs1049269
SPOCK2
1.000 0.080 10 72060243 3 prime UTR variant A/G snv 0.64 1
rs1245560
SPOCK2
1.000 0.080 10 72077662 intron variant A/C snv 0.51 1
rs556493
STXBP5
1.000 0.080 6 147228161 intron variant A/C;G;T snv 1
rs5743827
TLR6 ; TLR1
1.000 0.080 4 38825904 3 prime UTR variant C/T snv 0.27 1
rs17135889
ABCA3
0.925 0.080 16 2337259 intron variant G/A snv 0.11 2
rs371131106
ACE
0.925 0.120 17 63485346 missense variant A/G snv 8.4E-05 1.6E-04 2
rs1610037
ADCYAP1
0.925 0.120 18 910634 3 prime UTR variant A/G snv 0.26 2
rs35320474
ADORA2A ; SPECC1L-ADORA2A ; ADORA2A-AS1
1.000 0.080 22 24441941 3 prime UTR variant -/T delins 2
rs2284017
CACNG2
0.925 0.120 22 36700882 intron variant T/C snv 0.44 2