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: rs587779420
rs587779420
1 1.000 0.160 2 188988100 missense variant G/A;C snv 0.800 1.000 26 1989 2017
dbSNP: rs587779436
rs587779436
1 1.000 0.160 2 188988608 missense variant G/C snv 0.800 1.000 26 1989 2017
dbSNP: rs587779464
rs587779464
1 1.000 0.160 2 188990317 missense variant G/A;T snv 0.800 1.000 26 1989 2017
dbSNP: rs587779465
rs587779465
1 1.000 0.160 2 189008126 missense variant G/A;T snv 0.800 1.000 26 1989 2017
dbSNP: rs587779468
rs587779468
1 1.000 0.160 2 188990123 missense variant G/A;C snv 0.800 1.000 26 1989 2017
dbSNP: rs587779471
rs587779471
1 1.000 0.160 2 189004090 missense variant G/A;T snv 0.800 1.000 26 1989 2017
dbSNP: rs587779473
rs587779473
1 1.000 0.160 2 189008099 missense variant G/A;T snv 0.800 1.000 26 1989 2017
dbSNP: rs587779476
rs587779476
1 1.000 0.160 2 188995056 missense variant G/A snv 0.800 1.000 26 1989 2017
dbSNP: rs587779483
rs587779483
1 1.000 0.160 2 189004046 missense variant G/T snv 0.800 1.000 26 1989 2017
dbSNP: rs587779486
rs587779486
1 1.000 0.160 2 189002991 missense variant G/T snv 0.800 1.000 26 1989 2017
dbSNP: rs587779493
rs587779493
1 1.000 0.160 2 188998675 missense variant G/A snv 0.800 1.000 26 1989 2017
dbSNP: rs587779504
rs587779504
1 1.000 0.160 2 189008960 missense variant G/A snv 0.800 1.000 26 1989 2017
dbSNP: rs587779505
rs587779505
1 1.000 0.160 2 189004028 missense variant G/A snv 0.800 1.000 26 1989 2017
dbSNP: rs587779517
rs587779517
1 1.000 0.160 2 189004258 missense variant G/A snv 0.800 1.000 26 1989 2017
dbSNP: rs587779521
rs587779521
1 1.000 0.160 2 189008134 missense variant G/A snv 0.800 1.000 26 1989 2017
dbSNP: rs587779522
rs587779522
1 1.000 0.160 2 188997736 missense variant G/C snv 0.800 1.000 26 1989 2017
dbSNP: rs587779523
rs587779523
1 1.000 0.160 2 188995091 missense variant G/A snv 0.800 1.000 26 1989 2017
dbSNP: rs587779533
rs587779533
1 1.000 0.160 2 188989433 missense variant G/C;T snv 0.800 1.000 26 1989 2017
dbSNP: rs587779548
rs587779548
1 1.000 0.160 2 189005413 missense variant G/A;C snv 0.800 1.000 26 1989 2017
dbSNP: rs587779552
rs587779552
1 1.000 0.160 2 189005450 missense variant G/A snv 0.800 1.000 26 1989 2017
dbSNP: rs587779553
rs587779553
1 1.000 0.160 2 189008107 missense variant G/A;C;T snv 0.800 1.000 26 1989 2017
dbSNP: rs587779555
rs587779555
1 1.000 0.160 2 188989442 missense variant G/A snv 0.800 1.000 26 1989 2017
dbSNP: rs587779559
rs587779559
1 1.000 0.160 2 189004348 missense variant G/A;C snv 0.800 1.000 26 1989 2017
dbSNP: rs587779566
rs587779566
1 1.000 0.160 2 189004126 missense variant G/C snv 0.800 1.000 26 1989 2017
dbSNP: rs587779571
rs587779571
1 1.000 0.160 2 189004330 missense variant G/T snv 0.800 1.000 26 1989 2017