Source: ALL
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: rs767910122
rs767910122
17 0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 0.020 1.000 2 2011 2017
dbSNP: rs199472718
rs199472718
2 1.000 0.120 11 2572102 missense variant A/C;G snv 0.010 1.000 1 2013 2013
dbSNP: rs1554920808
rs1554920808
3 1.000 0.120 11 2776991 missense variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs199473103
rs199473103
3 0.925 0.120 3 38606102 missense variant A/G snv 0.010 1.000 1 2008 2008
dbSNP: rs267606782
rs267606782
EMD
4 0.925 0.120 X 154379485 start lost A/G snv 0.010 1.000 1 2015 2015
dbSNP: rs143149582
rs143149582
1 11 2588801 missense variant C/A snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs199473470
rs199473470
2 1.000 0.120 11 2583472 missense variant C/A snv 0.010 1.000 1 2010 2010
dbSNP: rs1247665387
rs1247665387
14 0.807 0.360 16 74774623 missense variant C/A snv 7.0E-06 0.700 0
dbSNP: rs566251672
rs566251672
2 1.000 0.120 3 38587437 missense variant C/A;T snv 4.0E-06; 1.6E-05 0.010 1.000 1 2013 2013
dbSNP: rs199472730
rs199472730
5 0.882 0.120 11 2572895 missense variant C/G;T snv 0.020 1.000 2 2011 2018
dbSNP: rs104894585
rs104894585
5 0.851 0.120 17 70175263 missense variant C/G;T snv 0.010 1.000 1 2007 2007
dbSNP: rs199473605
rs199473605
7 0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs199473442
rs199473442
3 1.000 0.120 11 2445103 missense variant C/G;T snv 0.700 0
dbSNP: rs104894485
rs104894485
4 0.882 0.080 15 73325378 missense variant C/T snv 3.6E-05 7.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs1554430943
rs1554430943
4 0.925 0.160 7 150974821 missense variant C/T snv 0.700 0
dbSNP: rs201943194
rs201943194
38 0.683 0.480 7 21710596 stop gained C/T snv 8.5E-05 8.4E-05 0.700 0
dbSNP: rs868064163
rs868064163
13 1.000 0.040 3 179586552 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs794728448
rs794728448
17 0.724 0.280 7 150948445 frameshift variant CT/G delins 0.020 1.000 2 2011 2017
dbSNP: rs1554919471
rs1554919471
4 0.925 0.200 11 2768861 frameshift variant G/- delins 0.700 1.000 1 2018 2018
dbSNP: rs11551437
rs11551437
3 1.000 0.080 2 47161833 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs121434500
rs121434500
5 0.851 0.120 20 33410203 missense variant G/A snv 2.0E-05 1.4E-05 0.010 1.000 1 2008 2008
dbSNP: rs121912504
rs121912504
6 0.851 0.200 7 150951711 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs1254179611
rs1254179611
3 1.000 0.120 7 150958295 missense variant G/A snv 0.010 1.000 1 2002 2002
dbSNP: rs139467962
rs139467962
2 1.000 0.120 20 33412702 missense variant G/A snv 1.6E-05 4.9E-05 0.010 1.000 1 2013 2013
dbSNP: rs199472756
rs199472756
3 0.925 0.120 11 2583486 missense variant G/A snv 0.010 1.000 1 2012 2012