Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs281865407 1.000 1 93996137 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 1
rs749526785 0.925 0.080 1 93997842 splice region variant GCCCCAGGGCCAACT/- delins 6.8E-05 2
rs61748521 1.000 1 93997869 missense variant G/A;C snv 4.0E-06; 1.1E-04 1
rs886044764 1.000 1 93997877 missense variant T/C snv 1
rs61750659 1.000 1 93997904 missense variant A/G snv 6.8E-05 1.4E-05 1
rs61753046 0.925 0.040 1 93997932 stop gained G/A;T snv 5.2E-05; 4.0E-06 2
rs886044763 1.000 1 93997943 missense variant G/A;T snv 1.2E-05; 4.0E-06 1
rs61753045 1.000 1 93997981 stop gained G/T snv 1
rs1800555 1.000 0.040 1 93998061 missense variant C/T snv 1.1E-02 1.0E-02 1
rs886044762 1.000 1 93998075 missense variant T/C snv 1
rs281865405 1.000 1 94000836 missense variant T/C snv 1
rs61751384 0.925 0.080 1 94000866 missense variant C/T snv 2.4E-05 4.9E-05 2
rs61750656 1.000 1 94000867 missense variant A/G snv 4.0E-06 7.0E-06 1
rs61750655 1.000 1 94000869 missense variant C/A;T snv 5.6E-05 1
rs61750654 0.925 0.120 1 94000870 stop gained G/A snv 2.0E-05 7.0E-06 5
rs61753044 1.000 0.080 1 94000878 missense variant C/T snv 1
rs61750653 1.000 1 94000900 missense variant G/A;T snv 8.0E-06; 8.0E-06 1
rs61750652 1.000 1 94000924 missense variant C/T snv 4.0E-06 7.0E-06 1
rs61753043 1.000 1 94001000 splice donor variant G/C snv 4.0E-06 7.0E-06 1
rs61750651 1.000 1 94001005 missense variant T/C snv 8.0E-06 1
rs61748520 1.000 1 94001046 synonymous variant C/G;T snv 4.0E-06; 1.6E-05 1
rs62642565 1.000 1 94001059 stop gained C/T snv 1
rs886044761 1.000 1 94001062 missense variant A/G snv 1
rs62642564 0.925 0.040 1 94001068 missense variant C/G;T snv 1.5E-03 2
rs2297669 1.000 1 94001069 missense variant G/A;T snv 1.6E-05 1