Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2505568 0.851 0.160 10 36522408 non coding transcript exon variant T/A snv 0.56 4
rs1846594 0.925 0.120 3 113197356 intergenic variant G/A;T snv 2
rs2472299 1.000 0.040 15 74741059 intergenic variant A/G;T snv 2
rs74676849 1.000 0.040 7 11849866 intergenic variant A/G snv 2.6E-02 1
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs145579007
ACE
0.925 0.080 17 63496503 missense variant G/A snv 1.0E-04 1.0E-04 2
rs750712925
ACE
0.925 0.080 17 63477227 missense variant G/A;C;T snv 3.2E-05 2
rs670957
ACTC1 ; LOC101928174
0.925 0.080 15 34797231 intron variant G/A snv 0.45 2
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs755661906
ANKRD1
1.000 0.040 10 90917732 missense variant C/T snv 1
rs755559514
APLN
0.925 0.040 X 129648648 missense variant T/C;G snv 1.2E-05; 6.1E-06 3
rs2781666
ARG1
0.790 0.280 6 131572419 intron variant G/T snv 0.45 8
rs1805105
AXIN1
0.776 0.280 16 346264 synonymous variant A/G snv 0.61 0.69 11
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs397516881
BAG3
0.827 0.120 10 119676917 missense variant G/A snv 7
rs2234962
BAG3
1.000 0.040 10 119670121 missense variant T/C snv 0.17 0.15 3
rs387906876
BAG3
0.925 0.040 10 119676984 missense variant G/A snv 2
rs397514507
BAG3
0.925 0.040 10 119676939 missense variant T/C snv 2
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 7
rs3763317
BTNL2
1.000 0.040 6 32409011 upstream gene variant C/T snv 0.49 2
rs9268492
BTNL2 ; TSBP1-AS1
0.882 0.200 6 32407503 non coding transcript exon variant C/G snv 0.31 3
rs9268494
BTNL2 ; TSBP1-AS1
0.882 0.200 6 32407575 non coding transcript exon variant A/C;T snv 0.32 3