Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs11887534 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs3736228 0.752 0.400 11 68433827 missense variant C/T snv 0.13 0.11 13