Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137854619 0.925 0.120 3 38550917 missense variant C/T snv 2.7E-04 7.7E-05 1
rs137854614 0.882 0.120 3 38550988 missense variant T/C snv 1
rs137854615 0.851 0.120 3 38550989 missense variant A/G snv 1
rs727504495 1.000 0.080 3 38550998 missense variant C/A;T snv 4.0E-06; 2.0E-05 1
rs199473317 0.882 0.120 3 38551003 missense variant T/C snv 1
rs137854601 0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 2
rs199473634 0.925 0.120 3 38551036 missense variant G/A snv 4.0E-05 7.7E-05 2
rs199473314 1.000 0.120 3 38551043 missense variant C/T snv 1.6E-05 2.1E-05 1
rs199473311 0.882 0.120 3 38551070 missense variant T/C snv 7.0E-06 1
rs199473632 1.000 0.120 3 38551072 missense variant T/C snv 1
rs199473310 1.000 0.120 3 38551076 missense variant T/A;C;G snv 1
rs199473309 1.000 0.080 3 38551082 missense variant C/A snv 1
rs199473631 0.925 0.120 3 38551085 missense variant C/T snv 1
rs199473308 1.000 0.120 3 38551090 missense variant A/T snv 1
rs199473307 1.000 0.120 3 38551091 missense variant G/A snv 1
rs199473629 1.000 0.080 3 38551144 missense variant C/T snv 1
rs199473305 0.925 0.080 3 38551145 missense variant C/T snv 1.4E-05 1
rs199473304 1.000 0.080 3 38551154 missense variant C/T snv 1
rs199473303 0.925 0.120 3 38551157 missense variant G/A;T snv 3.6E-05; 4.0E-06 1
rs193922726 1.000 0.080 3 38551188 missense variant G/A;C snv 6.0E-05 1
rs199473302 1.000 0.080 3 38551190 missense variant A/G snv 1
rs199473300 1.000 0.120 3 38551204 missense variant G/T snv 1.4E-05 1
rs199473299 1.000 0.080 3 38551208 missense variant T/C snv 1
rs199473628 1.000 0.080 3 38551231 missense variant T/C snv 1
rs199473298 1.000 0.080 3 38551238 missense variant C/T snv 4.0E-06 1