Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 7
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25 4
rs117758012
HOOK2 ; MAST1
1.000 0.080 19 12846836 intron variant C/T snv 4.1E-02 3
rs1858826
GNGT1
1.000 0.080 7 93719703 intron variant C/T snv 0.90 3
rs1973765
LSP1
1.000 0.080 11 1877434 intron variant T/C snv 0.37 3
rs6776003
RASA2
1.000 0.080 3 141547651 intron variant G/A snv 0.55 3
rs72755295
EXO1
1.000 0.080 1 241870961 intron variant A/G snv 2.1E-02 3
rs111342015
TTBK1
1.000 0.080 6 43259403 intron variant G/A;T snv 2
rs113701136 1.000 0.080 19 29786822 intergenic variant C/T snv 0.26 2
rs11977670
LOC107986854
1.000 0.080 7 140242504 downstream gene variant G/A snv 0.39 2
rs13260300 1.000 0.080 8 74567389 regulatory region variant C/T snv 0.67 2
rs310291 1.000 0.080 8 23801998 downstream gene variant G/A;C snv 2
rs3135724
FGFR2
1.000 0.080 10 121592706 intron variant C/G;T snv 2
rs3757322
CCDC170
1.000 0.080 6 151621059 3 prime UTR variant T/G snv 0.36 2
rs3853291 1.000 0.080 11 44347927 intergenic variant G/A;C snv 2
rs62061734
MAPT
1.000 0.080 17 45941122 intron variant T/A;C snv 2
rs62355902 1.000 0.080 5 56757896 intergenic variant A/T snv 0.15 2
rs6453204
SV2C
1.000 0.080 5 76143375 intron variant A/G snv 0.90 2
rs6473252 1.000 0.080 8 80887958 intergenic variant C/T snv 0.33 2
rs6756513 1.000 0.080 2 69945455 downstream gene variant G/A snv 0.26 2
rs6815814
TLR1
1.000 0.080 4 38814717 intron variant A/C snv 0.43 2
rs72932540
LOC338694 ; SMIM38
1.000 0.080 11 69154575 intron variant A/G snv 1.8E-03 2
rs745570 1.000 0.080 17 79807926 intergenic variant A/G snv 0.60 2
rs9397437 1.000 0.080 6 151631197 intergenic variant G/A snv 6.6E-02 2
rs10022462
PPM1K-DT
1.000 0.080 4 88322666 intron variant C/T snv 0.41 1