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
rs6271
DBH-AS1 ; DBH
1.000 0.040 9 133657152 missense variant C/T snv 4.6E-02 4.8E-02 5
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 4
rs2297322
SLC15A1
1.000 0.040 13 98723927 missense variant C/G;T snv 0.22 4
rs7240004 1.000 0.040 18 48868651 intergenic variant A/G snv 0.43 4
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs11064881
CIT
1.000 0.040 12 119709120 intron variant G/A snv 5.0E-02 3
rs12521868
IRF1-AS1
1.000 0.040 5 132448701 intron variant G/T snv 0.28 3
rs13001325
IL18R1 ; IL1RL1
1.000 0.040 2 102322576 intron variant C/T snv 0.30 3
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02 3
rs2097432 1.000 0.040 6 32622994 TF binding site variant T/C snv 0.27 3
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs4286721 1.000 0.040 5 40497502 intron variant G/A snv 0.64 3
rs6667605
LOC100996583
1.000 0.040 1 2571341 downstream gene variant C/T snv 0.53 3
rs670523
RIT1
1.000 0.040 1 155908941 intron variant A/G snv 0.48 3
rs7573065
SLC11A1
1.000 0.120 2 218381984 upstream gene variant C/A;T snv 3
rs867671924
ITGB3
1.000 0.080 17 47292176 missense variant C/A snv 3
rs10051722 1.000 0.040 5 130768383 intron variant A/C;G snv 2
rs10065637
ANKRD55
1.000 0.040 5 56143024 intron variant C/T snv 0.15 2
rs1042058
MAP3K8
1.000 0.040 10 30439172 synonymous variant T/C snv 0.51 0.45 2
rs10486483
SKAP2
1.000 0.040 7 26852821 intron variant G/A snv 0.21 2
rs10491434
IL7R
1.000 0.080 5 35877812 3 prime UTR variant A/G snv 0.32 2
rs10495903
THADA
1.000 0.040 2 43579779 intron variant C/T snv 0.13 2
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 2
rs1077773
KCCAT333
1.000 0.040 7 17403055 intron variant G/A;C snv 2