Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs755136231
rs755136231
1.000 0.160 5 13791995 frameshift variant TTTGGTTC/- del 2.0E-05 1.4E-05
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 2 2002 2006
dbSNP: rs878855279
rs878855279
3 180651492 frameshift variant TTGT/- delins
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs397515424
rs397515424
1.000 8 132632794 frameshift variant TT/- del 2.0E-05 7.0E-06
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs768881056
rs768881056
5 13876738 frameshift variant TT/- delins
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs1554255966
rs1554255966
7 775031 frameshift variant TGCCCCA/CCACCCTGGGT delins
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs1554269295
rs1554269295
7 21687485 frameshift variant TGAAAATGATTCATGATGCCATCAGAAACAGGAAGAAG/- delins
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs876657637
rs876657637
1.000 14 73671556 frameshift variant TATCTTT/- delins 1.4E-05
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 1 2011 2011
dbSNP: rs768986129
rs768986129
6 116628368 splice donor variant TAGG/- delins 1.2E-05 2.8E-05
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 3 2009 2013
dbSNP: rs587778821
rs587778821
3 180616873 frameshift variant TAC/A delins
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs878855280
rs878855280
3 180663913 frameshift variant TA/- delins
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs151107532
rs151107532
0.925 0.160 21 42486463 splice acceptor variant T/G snv 3.7E-04 4.7E-04
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 3 2013 2014
dbSNP: rs757801770
rs757801770
5 13883096 splice acceptor variant T/G snv
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 2 2002 2006
dbSNP: rs863224503
rs863224503
5 13708337 splice acceptor variant T/G snv
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 2 2002 2006
dbSNP: rs1554248617
rs1554248617
6 116622771 stop gained T/G snv
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs267607227
rs267607227
0.925 0.160 16 84154748 missense variant T/C;G snv
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs548521732
rs548521732
1.000 0.160 5 13839530 splice acceptor variant T/C snv 4.0E-05 2.8E-05
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 4 2002 2016
dbSNP: rs756235547
rs756235547
3 180659582 splice acceptor variant T/C snv 1.2E-04 8.4E-05
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 4 2011 2013
dbSNP: rs565076112
rs565076112
5 13922330 splice acceptor variant T/C snv 2.4E-05
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 2 2002 2006
dbSNP: rs769267893
rs769267893
5 13928180 splice acceptor variant T/C snv 4.0E-06
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 2 2002 2006
dbSNP: rs397514561
rs397514561
1.000 7 780097 missense variant T/C snv
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 1 2012 2012
dbSNP: rs577069249
rs577069249
3 180650140 intron variant T/C snv 5.0E-04
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 1.000 1 2011 2011
dbSNP: rs1060503064
rs1060503064
7 21854418 missense variant T/C snv
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs1553804100
rs1553804100
3 180647254 intron variant T/C snv
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs1554019966
rs1554019966
5 55232365 missense variant T/C snv
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0
dbSNP: rs727502974
rs727502974
5 13792055 missense variant T/C snv 2.4E-05 7.7E-05
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.700 0