Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs502652 1.000 0.040 5 101043608 intergenic variant C/T snv 0.27 1
rs1277240795
OGA
1.000 0.040 10 101791382 missense variant G/C snv 7.0E-06 2
rs11191392
WBP1L
1.000 0.040 10 102767194 intron variant C/A snv 0.49 1
rs3740397
WBP1L ; CYP17A1-AS1 ; CYP17A1
1.000 0.040 10 102832918 3 prime UTR variant G/C snv 0.35 1
rs743572
CYP17A1
0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs12765002
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875591 intron variant C/T snv 0.24 2
rs3740393
BORCS7-ASMT ; AS3MT
0.776 0.280 10 102876898 intron variant G/C;T snv 10
rs12260436
CNNM2
1.000 0.040 10 102981357 intron variant A/C snv 0.29 1
rs1890184
CNNM2
1.000 0.040 10 102988702 intron variant A/C;T snv 1
rs77420391
NT5C2
1.000 0.040 10 103186066 intron variant G/A snv 8.9E-02 2
rs246914 1.000 0.040 5 103223706 intergenic variant T/C snv 0.17 1
rs1163085
INA
1.000 0.040 10 103279484 intron variant G/A snv 0.64 1
rs391236 1.000 0.040 5 103342372 intergenic variant A/G snv 0.24 1
rs2672852 1.000 0.040 2 103455652 intergenic variant C/T snv 0.44 1
rs4526367
MSRA
1.000 0.040 8 10355952 intron variant G/A snv 0.77 1
rs10034259
LINC02503
1.000 0.040 4 104012596 intron variant A/C snv 0.19 1
rs150491901 1.000 0.040 8 10468395 intergenic variant G/A;T snv 1
rs1562927768
KMT2E
0.790 0.080 7 105101476 frameshift variant AAAGA/- delins 15
rs1826787 1.000 0.040 10 105908635 downstream gene variant C/T snv 0.16 1
rs1426371
LOC105369965 ; WSCD2
1.000 0.040 12 108236003 intron variant G/A snv 0.20 3
rs4623951
DAO
0.925 0.080 12 108878275 intron variant C/G;T snv 3
rs2070587
DAO
0.882 0.080 12 108883967 intron variant T/G snv 0.32 5
rs2111902
DAO
0.925 0.080 12 108884971 intron variant T/A;G snv 0.40 3
rs3741775
DAO
0.925 0.080 12 108889827 intron variant A/C;G snv 3
rs3742020
MYO1H
1.000 0.040 12 109445449 non coding transcript exon variant T/C snv 0.33 1