Source: CLINVAR

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: rs864309680
rs864309680
1.000 0.200 X 40062174 frameshift variant TCTC/- del
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs864309702
rs864309702
1.000 0.200 X 40074207 frameshift variant AACT/- delins
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs397515625
rs397515625
0.882 0.200 21 43169160 missense variant C/A;T snv 4.0E-06
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.720 1.000 1 2013 2018
dbSNP: rs864309685
rs864309685
1.000 0.200 21 43169241 missense variant T/C;G snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs1114167311
rs1114167311
1.000 0.200 21 43172198 frameshift variant A/- del
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs397515623
rs397515623
0.925 0.200 21 43169259 missense variant C/T snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs144451841
rs144451841
1.000 0.200 11 111910331 missense variant C/A;T snv 1.2E-05
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs864309682
rs864309682
1.000 0.200 22 26607953 missense variant C/T snv 4.0E-06
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs147344332
rs147344332
1.000 0.200 22 25231737 missense variant T/G snv 1.1E-04 7.0E-05
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs864309683
rs864309683
1.000 0.200 22 25231710 missense variant T/C snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs74315489
rs74315489
0.925 0.200 22 25231617 stop gained C/T snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs886041410
rs886041410
0.925 0.200 22 25231717 missense variant G/A;T snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.710 1.000 0 2012 2012
dbSNP: rs74315490
rs74315490
0.925 0.200 22 25207069 missense variant G/A;C snv 2.0E-05; 1.2E-05
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs864309700
rs864309700
1.000 0.200 22 25207210 stop lost T/C snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs139353014
rs139353014
1.000 0.200 2 208163217 missense variant C/T snv 3.9E-03 2.3E-03
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs587778872
rs587778872
0.807 0.200 2 208128231 missense variant G/A;C snv 8.0E-06
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs864309689
rs864309689
1.000 0.200 2 208128399 frameshift variant GG/A delins
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs28931605
rs28931605
0.807 0.200 2 208124294 missense variant G/A;T snv 4.2E-06; 1.3E-05
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.720 1.000 1 2016 2017
dbSNP: rs864309701
rs864309701
1.000 0.200 2 208121749 frameshift variant -/C delins
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs1114167312
rs1114167312
1.000 0.200 3 186539588 missense variant AG/TT mnv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs121908096
rs121908096
0.827 0.320 2 218814186 missense variant C/A;T snv 8.0E-06; 2.9E-04
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs587778779
rs587778779
0.807 0.240 2 218814379 splice acceptor variant G/A;T snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs886556800
rs886556800
0.827 0.320 2 218809576 splice acceptor variant G/T snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs1114167313
rs1114167313
1.000 0.200 6 10626489 missense variant T/C snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs1114167314
rs1114167314
1.000 0.200 6 10626564 frameshift variant ATCA/- delins
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0