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: rs1064793014
rs1064793014
1 94007707 missense variant T/C snv
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2014 2014
dbSNP: rs137853907
rs137853907
4 16000517 stop gained G/T snv 2.8E-05 8.4E-05
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2011 2011
dbSNP: rs1401818080
rs1401818080
8 43197027 splice region variant -/A delins 4.0E-06; 1.2E-05 1.4E-05
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2009 2009
dbSNP: rs1553190559
rs1553190559
1 94042790 missense variant A/T snv
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2013 2013
dbSNP: rs1553192432
rs1553192432
1 94060712 frameshift variant -/C delins
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2013 2013
dbSNP: rs1553263218
rs1553263218
1 197435404 frameshift variant -/G delins
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2007 2007
dbSNP: rs1554270834
rs1554270834
6 42722069 frameshift variant GCTGGGTC/- del
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2014 2014
dbSNP: rs1554824273
rs1554824273
RGR
10 84258712 3 prime UTR variant -/G delins
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 1999 1999
dbSNP: rs1555096248
rs1555096248
11 61950428 splice donor variant G/T snv
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2013 2013
dbSNP: rs199683808
rs199683808
1 68448644 missense variant G/A;C snv 1.6E-05
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2008 2008
dbSNP: rs372513650
rs372513650
4 15998489 splice acceptor variant C/G snv 3.0E-05 1.4E-05
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2015 2015
dbSNP: rs373331232
rs373331232
4 16023380 stop gained G/A;C snv 1.7E-05
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2014 2014
dbSNP: rs61752419
rs61752419
1 94042786 stop gained C/T snv
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2001 2001
dbSNP: rs758291149
rs758291149
3 101244651 stop gained A/G;T snv 2.4E-05 2.1E-05
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2010 2010
dbSNP: rs758316679
rs758316679
20 25339350 stop gained G/A snv 2.0E-05 7.0E-06
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2012 2012
dbSNP: rs782215106
rs782215106
10 47348733 missense variant C/A;T snv 4.0E-06; 3.2E-05
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2016 2016
dbSNP: rs782469310
rs782469310
10 47349721 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2016 2016
dbSNP: rs869312183
rs869312183
9 32541986 stop gained G/A snv
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2016 2016
dbSNP: rs869312184
rs869312184
1 94048898 frameshift variant C/- delins
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2016 2016
dbSNP: rs869312185
rs869312185
X 38287071 stop gained G/C snv
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2016 2016
dbSNP: rs869312186
rs869312186
1 216190298 stop gained C/A;G snv 4.0E-06
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2016 2016
dbSNP: rs869312187
rs869312187
19 54128351 stop gained C/A;T snv
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2016 2016
dbSNP: rs869312188
rs869312188
PHF3 ; EYS
6 63720752 frameshift variant -/CC delins
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2016 2016
dbSNP: rs878853382
rs878853382
6 79513293 frameshift variant TAGCTTC/- delins
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 1.000 1 2013 2013
dbSNP: rs111733491
rs111733491
2 169236027 missense variant C/A;G;T snv 8.0E-06; 3.6E-05
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.700 0