Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10013495 1.000 0.040 4 144584486 intron variant C/T snv 0.23 1
rs10014145
SLC39A8
1.000 0.040 4 102279420 intron variant A/G snv 0.31 1
rs10014396
SNCA
1.000 0.040 4 89791478 intron variant T/C snv 0.17 1
rs10014424
DNAJB14
1.000 0.040 4 99943207 intron variant G/A snv 6.2E-02 1
rs1001581
XRCC1
1.000 0.080 19 43561236 intron variant C/T snv 0.38 1
rs1001703993
PPOX
0.882 0.120 1 161170696 missense variant G/A;T snv 8.0E-06 1.4E-05 3
rs10017134
UGT2A2 ; UGT2A1
0.925 0.120 4 69591303 intron variant T/C snv 0.75 2
rs1001761
TYMS
1.000 0.080 18 662103 intron variant G/A snv 0.50 0.55 2
rs10019009
DMP1 ; LOC105377323
0.851 0.080 4 87661983 missense variant A/G;T snv 4.0E-06; 0.29 4
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs1002076
KIF1B
0.925 0.120 1 10378834 3 prime UTR variant G/A snv 0.33 2
rs1002149
GSR ; UBXN8
1.000 0.040 8 30728221 upstream gene variant G/T snv 0.20 1
rs1002212321
RIMS2
1.000 0.040 8 103931366 missense variant T/C snv 1
rs10022537
PROM1
0.925 0.080 4 16075214 intron variant A/T snv 0.70 2
rs10023113
CAMK2D
1.000 0.080 4 113625548 intron variant A/G snv 0.18 1
rs1002481
REV3L ; MFSD4B
0.882 0.080 6 111390819 intron variant T/A;G snv 3
rs1002630
CHN2
0.925 0.160 7 29388454 intron variant G/A snv 0.16 2
rs1002765
CHMP2B ; MIR4795
0.851 0.080 3 87227912 intron variant G/A;C snv 4
rs1002835
ITPR2
1.000 0.040 12 26539294 intron variant T/A snv 0.57 1
rs10029654
EGF
1.000 0.040 4 109940771 intron variant G/A snv 0.38 1
rs1003129577
WDR48
3 39094706 missense variant G/C snv 1
rs1003199
IL12B
1.000 0.160 5 159328558 intron variant C/T snv 0.43 1
rs10033029
PTPN13
1.000 0.040 4 86764643 missense variant T/C;G snv 9.4E-06; 8.0E-02 1
rs1003346
TMEM245
1.000 9 109053060 intron variant C/A snv 0.43 2
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8