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: rs1555817157
rs1555817157
0.742 0.280 20 25339320 frameshift variant TCTTCCTCAGGCG/- del
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 1.000 1 2018 2018
dbSNP: rs778361520
rs778361520
0.925 0.120 1 31728621 missense variant G/A snv 8.0E-06 2.1E-05
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 1.000 1 2017 2017
dbSNP: rs387907144
rs387907144
0.716 0.600 6 157181056 stop gained C/A;T snv
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 1.000 2 2012 2015
dbSNP: rs886039799
rs886039799
0.763 0.320 7 33273896 frameshift variant C/- del
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs375817528
rs375817528
0.776 0.160 11 65206824 splice region variant G/A snv 1.2E-04 1.2E-04
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs1555975523
rs1555975523
0.851 0.200 X 41534892 splice donor variant C/AT delins
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs398122845
rs398122845
1.000 0.080 X 41524036 splice acceptor variant T/A;C snv
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs1057518822
rs1057518822
1.000 0.080 12 88102888 stop gained G/A snv
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs137852834
rs137852834
0.763 0.280 12 88083936 stop gained T/A snv 5.5E-05 9.1E-05
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs757788894
rs757788894
0.882 0.120 16 1449081 missense variant C/T snv 4.0E-06
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs144078282
rs144078282
0.776 0.400 11 72302339 missense variant T/A;C snv 1.8E-04; 2.0E-04
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs200203460
rs200203460
0.776 0.400 11 72302312 stop gained G/A;C;T snv 2.8E-05
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs1558811557
rs1558811557
0.851 0.120 2 98377710 frameshift variant -/TCAGTGCTGCAGCCGGGGATCG delins
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs775796581
rs775796581
0.851 0.120 8 86666951 frameshift variant AGTCTGGG/- delins 5.2E-05 7.0E-05
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs765919785
rs765919785
0.882 0.080 21 45477409 splice acceptor variant A/G snv 8.2E-06 2.8E-05
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs1553281318
rs1553281318
0.882 0.120 1 226986536 frameshift variant -/A delins
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs1064795104
rs1064795104
0.790 0.440 2 72498492 stop gained A/C snv
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 1.000 2 2013 2014
dbSNP: rs61816761
rs61816761
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs1085307993
rs1085307993
0.716 0.440 5 161331056 missense variant C/T snv
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs796052505
rs796052505
0.724 0.440 5 162095551 missense variant G/A;C snv
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs1057518843
rs1057518843
0.790 0.240 14 87988523 missense variant C/T snv
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs377274761
rs377274761
0.776 0.240 14 87968393 missense variant C/T snv 8.0E-06 2.8E-05
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs752746786
rs752746786
0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 1.000 1 2016 2016
dbSNP: rs869312824
rs869312824
0.827 0.200 1 1804565 missense variant A/G snv
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 1.000 1 2016 2016