Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs11568818 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs7121 0.882 0.160 20 58903752 missense variant C/G;T snv 0.54 6
rs11672691 0.925 0.080 19 41479679 non coding transcript exon variant G/A snv 0.42 3
rs55958994 0.925 0.080 12 52907235 intron variant C/T snv 0.12 3