Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000113
IRGM
0.925 0.040 5 150860514 intron variant C/T snv 0.13 2
rs10001410
ADGRL3
1.000 0.040 4 61608511 intron variant C/A snv 0.55 1
rs1000256867
TP53
17 7673550 missense variant T/A;G snv 4.0E-06 1
rs1000283
HSD11B1 ; HSD11B1-AS1
0.925 0.080 1 209721316 intron variant G/A snv 0.18 2
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 7
rs1000592 1.000 0.040 2 118939624 upstream gene variant C/A snv 6.4E-03 1
rs1000597 0.925 0.120 7 30897563 intron variant T/A;C snv 2
rs10007052
RNF150
1.000 0.040 4 141084419 intron variant C/A snv 0.31 1
rs1000731
LOC105373170 ; TSNAX-DISC1 ; DISC1
1.000 0.040 1 231827745 intron variant C/T snv 0.23 1
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 1
rs10008257 0.925 0.040 4 94435177 intergenic variant G/A snv 0.63 2
rs10008492 1.000 0.120 4 38764099 intergenic variant C/G;T snv 1
rs10009145
LOC100507053 ; ADH4
1.000 0.080 4 99126778 intron variant G/A snv 0.39 0.34 1
rs10009228
CHRNA9
4 40354405 missense variant A/G snv 0.78 0.76 1
rs1000952
HTR3D
1.000 0.040 3 184038034 missense variant G/A;C;T snv 0.66; 3.6E-05; 4.0E-06 1
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs1001030257
PDE4D
5 58988559 missense variant T/C snv 2.0E-05 2.1E-05 1
rs10011025
GLRA3
1.000 0.120 4 174733072 intron variant A/C;G snv 1
rs10011540
UCP1
1.000 0.080 4 140568842 5 prime UTR variant T/G snv 0.10 1
rs1001164504
FIGLA
1.000 0.080 2 70790637 start lost A/G snv 3.5E-05 1
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10011796
ABCG2
0.882 0.160 4 88169725 intron variant T/C;G snv 1
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs10012946
WFS1
1.000 0.080 4 6291623 intron variant T/C snv 0.63 1
rs10013040
NEIL3
1.000 0.080 4 177309998 synonymous variant C/A snv 0.20 0.20 1