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: rs587783460
rs587783460
1 1.000 0.120 16 3793539 stop gained G/A snv 0.710 1.000 1 2016 2016
dbSNP: rs1555483834
rs1555483834
2 0.925 0.120 16 3778699 splice donor variant C/A;T snv 0.700 1.000 3 2006 2016
dbSNP: rs1567263114
rs1567263114
2 0.925 0.120 16 3729405 frameshift variant CT/- delins 0.700 1.000 3 2005 2011
dbSNP: rs200782888
rs200782888
2 0.925 0.120 16 3749626 splice donor variant C/G;T snv 0.700 1.000 3 2005 2008
dbSNP: rs797045037
rs797045037
1 1.000 0.120 16 3729433 missense variant T/C snv 0.700 1.000 1 2016 2016
dbSNP: rs11644721
rs11644721
1 1.000 0.120 16 3851010 splice acceptor variant C/A;T snv 0.700 0
dbSNP: rs1302427305
rs1302427305
2 0.925 0.120 16 3792074 stop gained G/A snv 0.700 0
dbSNP: rs147688139
rs147688139
1 1.000 0.120 16 3736812 stop gained A/G;T snv 4.0E-06 0.700 0
dbSNP: rs1555471323
rs1555471323
1 1.000 0.120 16 3729344 frameshift variant GTGTGCTGGG/- delins 0.700 0
dbSNP: rs1555471874
rs1555471874
1 1.000 0.120 16 3731350 stop gained T/A snv 0.700 0
dbSNP: rs1555472931
rs1555472931
1 1.000 0.120 16 3736101 stop gained C/A snv 0.700 0
dbSNP: rs1555472938
rs1555472938
2 0.925 0.120 16 3736119 frameshift variant CA/- delins 0.700 0
dbSNP: rs1555473491
rs1555473491
1 1.000 0.120 16 3738559 missense variant C/T snv 0.700 0
dbSNP: rs1555473668
rs1555473668
1 1.000 0.120 16 3739627 frameshift variant -/A delins 0.700 0
dbSNP: rs1555475352
rs1555475352
1 1.000 0.120 16 3745276 splice donor variant C/A snv 0.700 0
dbSNP: rs1555481030
rs1555481030
1 1.000 0.120 16 3767910 splice acceptor variant C/A snv 0.700 0
dbSNP: rs1555484797
rs1555484797
1 1.000 0.120 16 3782810 stop gained G/A snv 0.700 0
dbSNP: rs1555496560
rs1555496560
1 1.000 0.120 16 3850587 stop gained G/A snv 0.700 0
dbSNP: rs1555496581
rs1555496581
1 1.000 0.120 16 3850623 frameshift variant G/- del 0.700 0
dbSNP: rs1567276741
rs1567276741
1 1.000 0.120 16 3744899 frameshift variant G/- del 0.700 0
dbSNP: rs1567306142
rs1567306142
1 1.000 0.120 16 3778723 frameshift variant -/G delins 0.700 0
dbSNP: rs1567386034
rs1567386034
1 1.000 0.120 16 3879832 start lost TGTGCTGTCATTCGCCGAGAAACCGGGCGAGCTGAGTTTGGCTCTTTTGGGGTTGGGCGGTCCGTCCAGCAAGTTCTCAGCCATTTTCACCTGCTCGCGAAAACAGCCCCGGGCACGGGCGGCCGGGCCGGCGAGGGCCCGGACGGGGGTCGGGGGCCCTGCCGGCTGCGAGGGAGAGGAGCGAGCGCGGGCCGCGAGCGGGCGGGCGGGCGCCGAGGGAGAGGGAGGGCGCAGGCCGGGTGGGGGAGGCGGCGGCCAAATCTCAGCCACAGCAACAGCGCCCCGCAGC/- delins 0.700 0
dbSNP: rs267606752
rs267606752
2 0.925 0.120 16 3749631 missense variant C/T snv 0.700 0
dbSNP: rs398124145
rs398124145
1 1.000 0.120 16 3744893 splice donor variant C/T snv 0.700 0
dbSNP: rs398124146
rs398124146
12 0.742 0.360 16 3738617 missense variant G/A;C snv 0.700 0