Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7759127
HLA-B ; HLA-C
0.925 0.040 6 31273211 intron variant T/G snv 0.11 5
rs1040079
PACRG
0.882 0.040 6 162792995 intron variant A/G snv 0.31 3
rs3762318
C1orf141
0.925 0.040 1 67131436 intron variant G/A snv 0.83 3
rs1049432
TFAM
0.925 0.040 10 58395360 3 prime UTR variant G/C;T snv 2
rs11003124
MBL2
1.000 0.040 10 52772131 upstream gene variant T/G snv 0.30 2
rs12631031
PARL
0.925 0.040 3 183857982 intron variant G/A snv 0.12 2
rs2275606
LOC101928661 ; ADGB
0.925 0.040 6 146597814 intron variant G/A snv 7.7E-02 2
rs2853930
WASF5P ; HLA-B
1.000 0.040 6 31287647 non coding transcript exon variant A/C;T snv 0.10 2
rs532781899
FCN3
0.925 0.040 1 27373180 frameshift variant G/- delins 1.6E-02 1.8E-02 2
rs7298930
LRRK2
0.925 0.040 12 40325698 intron variant A/C;G;T snv 2
rs7653061
MIR4448 ; PARL
0.925 0.040 3 183886132 intron variant T/G snv 0.12 2
rs10100465
LOC105375721
1.000 0.040 8 117614040 intergenic variant G/A snv 0.23 1
rs10414149
SIGLEC5
1.000 0.040 19 51624491 intron variant A/G snv 0.30 1
rs10507522
LOC107984576
1.000 0.040 13 43904864 intron variant A/G snv 0.11 1
rs10817758
DELEC1
1.000 0.040 9 115381654 intron variant C/T snv 0.13 1
rs10982385 1.000 0.040 9 114730737 intergenic variant T/G snv 0.47 1
rs11174812
SLC2A13
1.000 0.040 12 40031285 intron variant C/T snv 0.36 1
rs13220141 1.000 0.040 6 146576497 intergenic variant A/T snv 8.2E-02 1
rs1587601 1.000 0.040 5 35254508 intergenic variant A/G snv 0.64 1
rs160451 1.000 0.040 8 89650713 intron variant T/C snv 0.56 1
rs16948876 1.000 0.040 16 50820507 intergenic variant G/A snv 6.2E-02 1
rs1873613
LINC02471 ; LINC02555
1.000 0.040 12 40158615 intron variant T/C snv 0.63 1
rs2023004
PRKN
1.000 0.040 6 162495517 intron variant T/C snv 0.31 1
rs2024825
C1orf141
1.000 0.040 1 67132294 intron variant T/A;C;G snv 1
rs2221593
BATF3
1.000 0.040 1 212700089 upstream gene variant C/A;G;T snv 1