Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61757955
GRB2
1.000 0.040 17 75318086 3 prime UTR variant A/G snv 4.2E-02 2
rs8753
POLR2A
1.000 0.040 17 7514323 non coding transcript exon variant C/T snv 1.4E-02 2
rs770617145
LOC100288866 ; NGFR
1.000 0.040 17 49512716 missense variant G/A snv 3.4E-05 1
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs1800067
ERCC4
0.716 0.320 16 13935176 missense variant G/A snv 5.6E-02 5.3E-02 17
rs2276466
ERCC4
0.732 0.320 16 13949318 3 prime UTR variant C/A;G snv 15
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36 13
rs11860248
RBBP6
0.882 0.040 16 24566445 intron variant T/G snv 0.27 5
rs769790595
IL4R
0.827 0.120 16 27360785 missense variant G/A;C snv 2.0E-05; 4.0E-06 5
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs2562152
RHBDF1
0.882 0.040 16 73898 intron variant A/T snv 0.67 4
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
rs13332653 0.882 0.040 16 24578078 intergenic variant T/G snv 0.11 3
rs2033214
RBBP6
0.882 0.040 16 24566199 intron variant T/G snv 0.14 3
rs9933544 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 3
rs372951639
NQO1
1.000 0.040 16 69718484 missense variant A/T snv 1.6E-05 3.5E-05 1
rs118101777
IDH2
0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs7164773
RORA
0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs865880036
MEIS2
0.827 0.040 15 37098156 missense variant A/C snv 1.3E-04 5
rs1801591
ETFA
0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 4
rs34988193
ANKDD1A
1.000 0.040 15 64943580 missense variant A/G snv 0.31 0.28 2
rs77633900
ETFA
1.000 0.040 15 76246118 intron variant G/C snv 6.3E-02 2