Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 18
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 15
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs174583 0.807 0.320 11 61842278 intron variant C/T snv 0.35 12
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 11
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 11
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 11
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs7758229 0.732 0.120 6 160419220 intron variant G/A;T snv 10
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 9
rs1665650 0.752 0.160 10 116727589 intron variant T/C snv 0.69 9
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 8
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 8
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 8
rs4072037 0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 7
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 7