Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4998386
GRIN2A
1.000 0.040 16 9976688 intron variant C/T snv 0.11 2
rs283413
ADH1B ; ADH1C
0.925 0.080 4 99347033 stop gained C/A;T snv 2
rs932546861
ADH1B ; ADH1C
1.000 0.040 4 99347032 frameshift variant C/- delins 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs6283
SLC2A9 ; DRD5
0.882 0.120 4 9783007 synonymous variant C/T snv 0.64 0.64 4
rs9516970
LOC105370324
1.000 0.040 13 97592635 intergenic variant G/A snv 0.56 1
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 4
rs766440014
PIK3CD
1.000 0.040 1 9715556 missense variant G/A snv 8.1E-06 1
rs11248060
DGKQ
1.000 0.040 4 970571 intron variant C/T snv 9.3E-02 1
rs1559085
CAST
0.925 0.040 5 96742998 intron variant A/G snv 9.4E-02 2
rs7118648
CCDC82
1.000 0.040 11 96375264 intron variant T/C;G snv 7.5E-02 1
rs591486
ERCC6L2
0.925 0.080 9 95887764 intron variant A/G snv 0.44 2
rs34311866
TMEM175
0.882 0.080 4 958159 missense variant T/C snv 0.18 0.14 6
rs765106589
PTCH1
1.000 0.040 9 95506446 missense variant C/T snv 4.0E-06 1
rs3798097
SEMA5A
1.000 0.040 5 9542417 intron variant C/T snv 0.23 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs34884217
TMEM175
0.925 0.080 4 950422 splice acceptor variant A/C snv 7.0E-02 6.8E-02 2
rs6599389
TMEM175
1.000 0.040 4 945325 intron variant G/A;T snv 1
rs142821586
TMEM175
1.000 0.040 4 945302 intron variant CT/- delins 3.5E-02 1
rs6599388
TMEM175
1.000 0.040 4 945299 intron variant C/T snv 0.28 1
rs7702187
SEMA5A
0.925 0.040 5 9332169 intron variant T/A snv 0.70 2
rs775174756
NDUFV2-AS1 ; NDUFV2
1.000 0.040 18 9126877 missense variant A/G snv 2.8E-05 1.4E-05 1
rs906807
NDUFV2
1.000 0.040 18 9117869 missense variant T/C;G snv 0.80; 4.0E-06 1