Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555969553
AR
0.925 0.200 X 67545438 stop gained C/T snv 2
rs1555982894
AR
0.925 0.160 X 67643409 splice donor variant T/C snv 2
rs1555990470
AR
0.925 0.200 X 67686046 missense variant G/A snv 2
rs1555995822
AR
0.925 0.200 X 67711569 missense variant G/A snv 2
rs1555996810
AR
0.925 0.200 X 67717480 missense variant T/C snv 2
rs1555996863
AR
0.925 0.200 X 67717600 missense variant G/A snv 2
rs1555997580
AR
0.925 0.200 X 67721873 stop gained C/T snv 2
rs1555998108
AR
0.925 0.200 X 67723776 missense variant A/T snv 2
rs1569314508
AR
0.925 0.200 X 67717623 splice donor variant G/C snv 2
rs200390780
AR
1.000 0.160 X 67546570 missense variant C/T snv 1.5E-03 1.1E-03 2
rs201934623
AR
0.925 0.160 X 67546320 missense variant C/T snv 4.5E-03 2.0E-03 2
rs372903533
AR
0.925 0.200 X 67711599 missense variant C/T snv 5.5E-06 9.5E-06 2
rs754201976
AR
0.925 0.160 X 67686088 missense variant G/A snv 5.5E-06 2
rs886039558
AR
0.925 0.200 X 67717561 stop gained C/T snv 2
rs886041132
AR
0.925 0.160 X 67722943 missense variant C/T snv 2
rs886041352
AR
0.925 0.160 X 67717618 missense variant A/C snv 2
rs1057521122
AR
1.000 0.160 X 67722881 missense variant A/G snv 1
rs1057523747
AR
1.000 0.160 X 67717562 missense variant G/A;T snv 1
rs1199988820
AR
1.000 0.160 X 67545363 stop gained C/G;T snv 7.3E-05 1
rs1254203917
AR
1.000 0.160 X 67721881 missense variant G/T snv 5.5E-06 1
rs1355285524
AR
1.000 0.160 X 67546480 missense variant A/G snv 1.8E-05 1.0E-05 1
rs137852563
AR
1.000 0.160 X 67711673 stop gained G/A snv 5.7E-06 1
rs137852566
AR
1.000 0.160 X 67686012 stop gained A/T snv 1
rs137852568
AR
1.000 0.160 X 67723728 stop gained A/T snv 1
rs137852570
AR
1.000 0.160 X 67721876 missense variant A/G snv 1