Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10819689
STX17-AS1 ; LOC101928438
1.000 0.080 9 99637981 intron variant C/T snv 0.20 1
rs11788118
STX17-AS1 ; LOC107987012
1.000 0.080 9 99575049 intron variant G/A snv 0.19 1
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2072450
GRIN2A
0.925 0.160 16 9821855 intron variant C/A snv 9.4E-02 2
rs4690229
DGKQ
1.000 0.080 4 976936 intron variant A/T snv 0.39 1
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs8023715 1.000 0.080 15 97064451 intergenic variant C/A;T snv 1
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs3733345
DGKQ
1.000 0.080 4 960459 3 prime UTR variant G/A;T snv 1
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs6601327 1.000 0.080 8 9538022 intergenic variant G/A snv 0.56 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
rs1133906
SAMD9L
0.925 0.080 7 93135669 synonymous variant C/T snv 0.22 0.28 2
rs11578098
EVI5
1.000 0.080 1 92653853 intron variant G/A snv 0.20 1
rs6662618 0.882 0.200 1 92469854 downstream gene variant T/G snv 0.75 3
rs12753920 1.000 0.080 1 92200342 upstream gene variant A/G snv 0.31 1
rs597325
BACH2
0.925 0.160 6 90292775 intron variant A/G snv 0.69 2
rs9515692 1.000 0.080 13 90141725 intergenic variant C/T snv 0.35 1
rs73846279 1.000 0.080 3 89842195 intergenic variant G/A;T snv 1
rs16900627
RIPK2
0.882 0.160 8 89790767 3 prime UTR variant A/G snv 0.17 4
rs16900617
RIPK2
1.000 0.080 8 89790263 synonymous variant A/G snv 2.1E-02 6.0E-02 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs2234767
FAS ; ACTA2
0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs4945
MFGE8
0.925 0.120 15 88913313 missense variant G/T snv 0.38 0.31 2