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: rs1554069793
rs1554069793
1 1.000 0.120 5 78781927 stop gained C/A snv 0.700 1.000 1 1996 1996
dbSNP: rs1554069808
rs1554069808
1 1.000 0.120 5 78781976 splice acceptor variant T/C snv 0.700 1.000 1 2007 2007
dbSNP: rs1554074118
rs1554074118
1 1.000 0.120 5 78839350 splice region variant A/G snv 0.700 1.000 2 2008 2015
dbSNP: rs1554074124
rs1554074124
1 1.000 0.120 5 78839361 frameshift variant G/- del 0.700 1.000 1 2014 2014
dbSNP: rs1554074132
rs1554074132
1 1.000 0.120 5 78839401 missense variant C/T snv 0.700 1.000 2 2014 2017
dbSNP: rs1554074135
rs1554074135
1 1.000 0.120 5 78839407 frameshift variant -/G delins 0.700 1.000 1 2007 2007
dbSNP: rs1554079265
rs1554079265
1 1.000 0.120 5 78885596 stop gained C/T snv 0.700 1.000 1 2007 2007
dbSNP: rs1554079268
rs1554079268
1 1.000 0.120 5 78885599 missense variant A/T snv 0.700 1.000 2 2014 2015
dbSNP: rs1554079284
rs1554079284
1 1.000 0.120 5 78885647 missense variant A/G snv 0.700 1.000 4 2000 2015
dbSNP: rs1554079296
rs1554079296
1 1.000 0.120 5 78885667 stop gained C/T snv 0.700 1.000 1 2015 2015
dbSNP: rs1554079302
rs1554079302
1 1.000 0.120 5 78885690 frameshift variant C/- delins 0.700 1.000 4 2007 2017
dbSNP: rs1554079312
rs1554079312
1 1.000 0.120 5 78885731 missense variant A/C snv 0.700 1.000 1 2013 2013
dbSNP: rs1554079318
rs1554079318
1 1.000 0.120 5 78885760 stop gained C/T snv 0.700 1.000 3 2007 2016
dbSNP: rs1554079320
rs1554079320
1 1.000 0.120 5 78885764 missense variant A/G snv 0.800 1.000 18 1991 2015
dbSNP: rs1554086368
rs1554086368
1 1.000 0.120 5 78955306 missense variant A/T snv 0.700 1.000 1 2007 2007
dbSNP: rs1554086370
rs1554086370
1 1.000 0.120 5 78955308 frameshift variant -/AA delins 0.700 1.000 1 2015 2015
dbSNP: rs1554086414
rs1554086414
1 1.000 0.120 5 78955428 stop gained A/C;T snv 0.700 1.000 3 2004 2014
dbSNP: rs1554086417
rs1554086417
1 1.000 0.120 5 78955439 frameshift variant AGTAT/CTTCAGG;CTTGACTTCAGG delins 0.700 1.000 2 2011 2012
dbSNP: rs1554086431
rs1554086431
1 1.000 0.120 5 78955477 missense variant T/C snv 0.700 1.000 12 1991 2012
dbSNP: rs1554087395
rs1554087395
1 1.000 0.120 5 78964446 frameshift variant TA/- delins 0.700 1.000 1 2015 2015
dbSNP: rs1554087406
rs1554087406
1 1.000 0.120 5 78964470 frameshift variant GTTGAAT/- delins 0.700 1.000 1 2007 2007
dbSNP: rs1554087423
rs1554087423
1 1.000 0.120 5 78964532 missense variant A/G snv 0.800 1.000 17 1991 2017
dbSNP: rs1554087439
rs1554087439
1 1.000 0.120 5 78964573 missense variant T/A snv 0.700 1.000 3 2007 2015
dbSNP: rs1554087441
rs1554087441
1 1.000 0.120 5 78964574 missense variant G/C snv 0.700 1.000 1 2014 2014
dbSNP: rs1554087445
rs1554087445
1 1.000 0.120 5 78964595 missense variant C/T snv 0.700 1.000 2 2007 2007