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: 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
dbSNP: rs79006549
rs79006549
1.000 0.200 3 111122207 missense variant A/C;G snv 1.9E-03
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: rs864309532
rs864309532
0.807 0.360 X 134393952 missense variant G/A snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs797045905
rs797045905
0.851 0.360 2 135164629 stop gained T/G snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs781984979
rs781984979
0.851 0.240 1 145912346 stop gained G/A snv 4.0E-06
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs781939614
rs781939614
0.851 0.240 1 145916914 stop gained G/A snv 4.0E-06
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs1114167309
rs1114167309
1.000 0.200 1 147908028 missense variant T/C snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs864309684
rs864309684
1.000 0.200 1 147908040 frameshift variant -/T delins
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs864309677
rs864309677
1.000 0.200 1 147908074 missense variant C/T snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs864309688
rs864309688
0.882 0.200 1 147908089 missense variant G/C snv 7.0E-06
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs864309703
rs864309703
1.000 0.200 1 147908106 missense variant G/A;C;T snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs1114167310
rs1114167310
1.000 0.200 1 147908439 missense variant G/A snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs864309690
rs864309690
0.925 0.200 10 17229436 frameshift variant C/- delins
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs864309679
rs864309679
NHS
1.000 0.200 X 17726875 frameshift variant G/- delins
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs111534978
rs111534978
NHS
1.000 0.200 X 17727793 stop gained C/A;T snv 4.4E-05
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: rs1114167308
rs1114167308
1.000 0.200 13 20142823 missense variant T/G snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs864309687
rs864309687
0.925 0.200 13 20143029 missense variant G/A snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs864309691
rs864309691
0.925 0.200 13 20143113 missense variant G/A snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
dbSNP: rs1114167307
rs1114167307
0.851 0.200 13 20143233 missense variant G/A snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 0
dbSNP: rs864309694
rs864309694
1.000 0.200 13 20143282 missense variant C/G snv
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.700 1.000 1 2016 2016
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: 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