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: rs137852488
rs137852488
1 1.000 0.120 X 134475257 missense variant G/C snv 0.810 1.000 16 1983 2014
dbSNP: rs137852483
rs137852483
1 1.000 0.120 X 134490192 missense variant T/A snv 0.810 1.000 15 1983 2014
dbSNP: rs137852480
rs137852480
1 1.000 0.120 X 134473453 missense variant T/C snv 0.800 1.000 15 1983 2014
dbSNP: rs137852481
rs137852481
1 1.000 0.120 X 134475268 missense variant C/A snv 0.800 1.000 15 1983 2014
dbSNP: rs137852486
rs137852486
1 1.000 0.120 X 134498670 missense variant T/G snv 0.800 1.000 15 1983 2014
dbSNP: rs137852487
rs137852487
1 1.000 0.120 X 134475255 missense variant G/A snv 0.800 1.000 15 1983 2014
dbSNP: rs137852490
rs137852490
1 1.000 0.120 X 134500030 missense variant C/G snv 0.800 1.000 15 1983 2014
dbSNP: rs137852491
rs137852491
1 1.000 0.120 X 134473465 missense variant G/A snv 4.4E-05 0.800 1.000 15 1983 2014
dbSNP: rs137852492
rs137852492
1 1.000 0.120 X 134498433 missense variant G/T snv 0.800 1.000 15 1983 2014
dbSNP: rs137852493
rs137852493
1 1.000 0.120 X 134498431 missense variant C/T snv 0.800 1.000 15 1983 2014
dbSNP: rs137852496
rs137852496
1 1.000 0.120 X 134493533 missense variant T/A snv 0.800 1.000 15 1983 2014
dbSNP: rs267606863
rs267606863
1 1.000 0.120 X 134498655 missense variant G/A;C snv 0.800 1.000 15 1983 2014
dbSNP: rs137852497
rs137852497
2 0.925 0.200 X 134498412 stop gained C/A;T snv 4.4E-05 0.710 1.000 1 2008 2008
dbSNP: rs137852495
rs137852495
2 0.925 0.120 X 134475216 missense variant T/C snv 0.700 1.000 15 1983 2014
dbSNP: rs1556026984
rs1556026984
4 0.925 0.120 X 134475194 missense variant G/C snv 0.700 1.000 15 1983 2014
dbSNP: rs137852489
rs137852489
2 0.925 0.160 X 134486471 stop gained C/A;T snv 2.4E-05 0.700 1.000 3 1990 1997
dbSNP: rs1556030169
rs1556030169
2 0.925 0.160 X 134498683 frameshift variant -/T delins 0.700 1.000 3 2000 2017
dbSNP: rs1135401801
rs1135401801
1 1.000 0.120 X 134473378 missense variant G/T snv 0.700 0
dbSNP: rs137852494
rs137852494
2 0.925 0.160 X 134475197 stop gained C/G;T snv 0.700 0
dbSNP: rs137852503
rs137852503
1 1.000 0.120 X 134493524 missense variant G/A snv 0.700 0
dbSNP: rs137852505
rs137852505
1 1.000 0.120 X 134493564 stop gained T/G snv 0.700 0
dbSNP: rs1569354918
rs1569354918
1 1.000 0.120 X 134473357 splice acceptor variant A/T snv 0.700 0
dbSNP: rs1569360089
rs1569360089
1 1.000 0.120 X 134498441 splice region variant G/A snv 0.700 0
dbSNP: rs1569360139
rs1569360139
1 1.000 0.120 X 134498689 splice region variant G/A snv 0.700 0
dbSNP: rs369065223
rs369065223
2 0.925 0.160 X 134486514 stop gained C/G;T snv 5.5E-06 0.700 0