Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 8
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 6
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 6
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs1456649
FMN2
1 240288305 intron variant G/C snv 3.0E-03 5
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs4495740
DOCK7
1 62658794 intron variant T/G snv 0.34 5
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs9436735
LEPR ; LEPROT
1 65419378 upstream gene variant C/G snv 2.5E-02 5
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4