Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852587
AR
0.925 0.160 X 67643387 missense variant T/A snv 2
rs137852588
AR
0.925 0.160 X 67643284 missense variant C/T snv 2
rs137852589
AR
0.925 0.160 X 67721857 missense variant G/A;T snv 5.5E-06 2
rs137852595
AR
0.925 0.160 X 67711653 missense variant C/A;T snv 2
rs137852600
AR
0.925 0.160 X 67717535 missense variant G/A;T snv 2
rs1410383824
AR
0.925 0.160 X 67546470 stop gained G/A;T snv 2
rs1555969553
AR
0.925 0.200 X 67545438 stop gained C/T snv 2
rs1555969684
AR
0.925 0.200 X 67545892 frameshift variant -/G delins 2
rs1555970004
AR
0.925 0.200 X 67546581 frameshift variant -/C delins 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
rs1569263557
AR
0.925 0.200 X 67545341 stop gained GCAGC/TT delins 2
rs1569264288
AR
0.925 0.200 X 67545971 frameshift variant -/CCGCTGTGCGTCCCAC delins 2
rs1569265331
AR
0.925 0.200 X 67546597 frameshift variant CTCG/- del 2
rs1569265470
AR
0.925 0.200 X 67546759 frameshift variant -/G delins 2
rs1569314508
AR
0.925 0.200 X 67717623 splice donor variant G/C snv 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