Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs228648
UTS2
0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs74315364
RNASEL
0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs851797
EXO1
0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs201765376
MTR
0.732 0.360 1 236838504 synonymous variant C/T snv 1.6E-05 1.4E-05 12
rs172378
C1QA
0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs2536
MTOR
0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 11
rs3754093
EXO1
0.776 0.240 1 241846814 upstream gene variant A/G snv 0.23 11
rs4645981
CASP9 ; DNAJC16
0.790 0.160 1 15524988 intron variant G/A;C snv 11
rs1380576
MDM4
0.763 0.240 1 204519150 intron variant G/C snv 0.57 10
rs2297595
DPYD
0.776 0.320 1 97699535 missense variant T/C snv 8.5E-02 8.1E-02 10
rs4846048
MTHFR ; C1orf167
0.752 0.280 1 11786195 3 prime UTR variant G/A snv 0.67 10
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 9
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 9
rs11801299
LOC105371692
0.807 0.200 1 204559956 downstream gene variant G/A snv 0.16 9
rs1635498
EXO1
0.807 0.160 1 241881973 missense variant C/A;G;T snv 0.96 9
rs1776148
EXO1
0.807 0.160 1 241879243 missense variant A/G snv 0.66 0.66 9
rs2266780
FMO3
0.827 0.280 1 171114102 missense variant A/G snv 0.15 0.14 9
rs5277
PACERR ; PTGS2
0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 9
rs7539542
ADIPOR1
0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58 9
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs4645978
CASP9 ; DNAJC16
0.827 0.120 1 15525539 intron variant C/A;T snv 8
rs751763046
EXO1
0.790 0.200 1 241885375 missense variant T/C snv 4.0E-06 8