Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs587784484
rs587784484
1 1.000 0.240 12 49185092 missense variant A/T snv 0.700 0
dbSNP: rs587784485
rs587784485
1 1.000 0.240 12 49186685 missense variant G/A snv 0.700 0
dbSNP: rs587784486
rs587784486
1 1.000 0.240 12 49186675 missense variant A/T snv 0.700 0
dbSNP: rs587784488
rs587784488
1 1.000 0.240 12 49185885 missense variant A/C;G snv 0.700 0
dbSNP: rs587784489
rs587784489
1 1.000 0.240 12 49185845 missense variant G/A snv 0.700 0
dbSNP: rs587784491
rs587784491
4 0.925 0.240 12 49186832 missense variant C/T snv 0.700 0
dbSNP: rs587784492
rs587784492
1 1.000 0.240 12 49185668 missense variant T/C snv 0.700 0
dbSNP: rs587784494
rs587784494
1 1.000 0.240 12 49185558 missense variant C/A;T snv 0.700 0
dbSNP: rs587784495
rs587784495
1 1.000 0.240 12 49185380 missense variant T/C snv 0.700 0
dbSNP: rs587784497
rs587784497
1 1.000 0.240 12 49185371 missense variant A/G snv 0.700 0
dbSNP: rs797046071
rs797046071
1 1.000 0.240 12 49185261 missense variant C/T snv 0.700 0
dbSNP: rs797046072
rs797046072
1 1.000 0.240 12 49186416 missense variant T/C snv 0.700 0
dbSNP: rs797046073
rs797046073
1 1.000 0.240 12 49185396 missense variant C/G snv 0.700 0
dbSNP: rs863224938
rs863224938
1 1.000 0.240 12 49186333 missense variant C/G;T snv 0.700 0
dbSNP: rs886043627
rs886043627
1 1.000 0.240 12 49185575 missense variant C/T snv 0.700 0