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: rs1555600876
rs1555600876
1 1.000 17 43124027 inframe deletion ACT/- del 0.700 1.000 18 1995 2014
dbSNP: rs751656678
rs751656678
1 1.000 17 43093028 missense variant G/A snv 4.0E-06 7.0E-06 0.700 1.000 15 2003 2017
dbSNP: rs45444999
rs45444999
1 1.000 17 43063882 missense variant C/A;T snv 0.700 1.000 13 2001 2019
dbSNP: rs397509035
rs397509035
1 1.000 17 43092409 stop gained G/A;C snv 0.700 1.000 3 2005 2016
dbSNP: rs80356873
rs80356873
1 1.000 17 43045734 stop gained G/A;T snv 0.700 1.000 3 2005 2012
dbSNP: rs1057517637
rs1057517637
1 1.000 17 43047669 frameshift variant -/C delins 4.0E-06 0.700 1.000 2 2000 2016
dbSNP: rs1555592956
rs1555592956
1 1.000 17 43094662 frameshift variant A/- delins 0.700 1.000 2 2001 2017
dbSNP: rs1555593294
rs1555593294
1 1.000 17 43094832 inframe deletion TAC/- del 0.700 1.000 2 1999 2011
dbSNP: rs397507239
rs397507239
1 1.000 17 43067614 stop gained T/A;G snv 4.0E-06; 3.2E-05 0.700 1.000 2 2012 2015
dbSNP: rs397509230
rs397509230
1 1.000 17 43063878 stop gained A/C;T snv 0.700 1.000 2 2009 2014
dbSNP: rs80357922
rs80357922
1 1.000 17 43093535 frameshift variant G/- delins 0.700 1.000 2 2012 2016
dbSNP: rs1173155015
rs1173155015
1 1.000 17 43071026 stop gained C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs273898681
rs273898681
1 1.000 17 43093330 frameshift variant CTTTTTCTTCTCTT/- delins 0.700 1.000 1 2011 2011
dbSNP: rs273902792
rs273902792
1 1.000 17 43094683 stop gained A/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs397507216
rs397507216
1 1.000 17 43092028 frameshift variant T/-;TT delins 0.700 1.000 1 2011 2011
dbSNP: rs397509195
rs397509195
1 1.000 17 43071154 stop gained G/C snv 0.700 1.000 1 2012 2012
dbSNP: rs397509258
rs397509258
1 1.000 17 43051088 stop gained A/C;T snv 0.700 1.000 1 2000 2000
dbSNP: rs730880287
rs730880287
1 1.000 17 43071076 frameshift variant CT/GGC delins 0.700 1.000 1 2016 2016
dbSNP: rs80357043
rs80357043
1 1.000 17 43067628 missense variant G/A snv 7.0E-06 0.700 1.000 1 2010 2010
dbSNP: rs80357577
rs80357577
1 1.000 17 43092133 frameshift variant AA/- del 0.700 1.000 1 2001 2001
dbSNP: rs80357782
rs80357782
1 1.000 17 43094008 frameshift variant G/- delins 0.700 1.000 1 2014 2014
dbSNP: rs80358019
rs80358019
1 1.000 17 43091034 splice acceptor variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs80358070
rs80358070
1 1.000 17 43091033 splice acceptor variant C/T snv 0.700 1.000 1 2012 2012
dbSNP: rs878853285
rs878853285
1 1.000 17 43051119 splice acceptor variant T/- del 0.700 1.000 1 2013 2013
dbSNP: rs878853286
rs878853286
1 1.000 17 43051062 splice donor variant CCT/ATGTTG delins 0.700 1.000 1 2012 2012