Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200034765 10 69247416 missense variant C/T snv 1.2E-05 2.1E-05 1
rs201306926 4 140399004 missense variant T/C snv 3.6E-05 7.0E-06 1
rs201435914 19 53636878 stop gained C/T snv 3.5E-04 3.6E-04 1
rs201805961 20 25292483 missense variant A/G snv 2.4E-05 2.1E-05 1
rs202070666 X 154460239 missense variant G/A snv 2.2E-04 6.5E-04 1
rs370433088 20 62322314 missense variant C/T snv 1.0E-04 1.0E-04 1
rs375633720 4 8601494 missense variant C/T snv 2.8E-05 4.2E-05 1
rs376253982 X 48966313 splice region variant C/A snv 2.0E-04 2.1E-04 1
rs377035972 14 24155679 missense variant G/A snv 5.6E-05 9.8E-05 1
rs377314861 18 21440307 missense variant C/T snv 6.3E-06 1
rs537353127 11 61273265 stop gained G/A;C;T snv 4.0E-06; 4.0E-06; 8.0E-06 1
rs540351799 1 29325243 missense variant A/C snv 1.2E-05 1.4E-05 1
rs559634261 1 39318497 missense variant G/A snv 2.0E-05 1
rs559788899 1 29303909 missense variant C/T snv 2.8E-05 1.4E-05 1
rs746040003 13 114018810 frameshift variant TCAG/- delins 1.6E-05 1
rs747141054 8 42973316 missense variant G/A snv 2.4E-05 4.9E-05 1
rs747262678 1 228279343 missense variant C/T snv 1.2E-05 1.4E-05 1
rs747762087 3 73384465 missense variant T/A;G snv 7.0E-06 1
rs747867083 1 19119624 missense variant C/T snv 4.0E-06 7.0E-06 1
rs748323629 1 19151825 missense variant T/C snv 8.0E-06 2.8E-05 1
rs752482499 14 23140529 missense variant C/T snv 1.2E-05 7.0E-06 1
rs755081350 1 39485559 missense variant G/A snv 1.6E-05 1
rs756386867 X 38160977 missense variant C/G snv 1.1E-05 9.5E-06 1
rs759951698 14 23139485 missense variant T/C snv 8.0E-06 7.0E-06 1
rs760297650 17 40022789 missense variant C/T snv 2.0E-05 2.1E-05 1