Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6336 0.827 0.120 1 156879126 missense variant C/T snv 4.2E-02 3.7E-02 5
rs6334 1.000 0.080 1 156876441 missense variant G/A;C;T snv 0.22; 4.0E-06 3
rs748653984 1.000 0.080 1 156868159 missense variant T/A;C snv 4.0E-06; 4.0E-06 2
rs778056858 1.000 0.080 1 156866944 missense variant T/C snv 8.0E-06 7.0E-06 2
rs775984846 1.000 1 156881535 missense variant G/A;C snv 3.5E-05 2
rs374918502 0.925 0.080 1 156880056 missense variant C/T snv 6.0E-05 7.6E-06 2
rs1007211 1.000 0.040 1 156860987 missense variant G/A snv 7.5E-03 9.4E-03 1
rs746049437 1.000 0.080 1 156876550 missense variant G/A snv 2.4E-05 7.0E-06 1
rs759637817 1.000 0.080 1 156881532 missense variant C/T snv 1.4E-05 1
rs121964866 1.000 0.080 1 156876496 missense variant G/A;C snv 2.0E-05 1
rs747711259 1.000 0.080 1 156868568 missense variant T/C snv 1.4E-05 1
rs371344688 1.000 0.040 1 156876514 missense variant C/G;T snv 6.4E-05; 2.4E-05 1
rs781698345 1 156873882 missense variant T/C snv 4.8E-06 2.1E-05 1
rs768876280 1.000 0.040 1 156881613 missense variant C/T snv 4.2E-06 2.1E-05 1
rs769854785 1 156871656 synonymous variant C/T snv 1
rs1009726086 1.000 0.040 1 156881499 missense variant C/T snv 1.4E-05 7.0E-06 1
rs763591781 1.000 0.040 1 156881481 missense variant C/T snv 5.1E-05 2.8E-05 1
rs759471657 1 156876418 stop gained G/A;C;T snv 1.2E-05; 4.0E-06 1
rs150579345 1 156876508 missense variant G/A snv 1.4E-04 9.8E-05 1
rs1293540396 1.000 1 156868557 synonymous variant C/T snv 1.8E-05 2.8E-05 1
rs199647144 1 156842109 missense variant T/C;G snv 8.8E-05; 4.0E-06 1
rs1032968973 1.000 0.080 1 156842164 synonymous variant A/G snv 4.0E-06 1.4E-05 1
rs926103 0.925 0.120 1 156815190 missense variant T/C snv 0.64 0.57 1