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: rs770374710
rs770374710
0.611 0.560 15 23645747 frameshift variant G/-;GG delins
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs1163944538
rs1163944538
0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs1352010373
rs1352010373
0.641 0.560 17 75489265 splice acceptor variant G/C snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs1276519904
rs1276519904
0.645 0.520 1 226071445 missense variant A/G snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs80338796
rs80338796
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs1553621496
rs1553621496
0.677 0.440 2 209976305 splice donor variant T/G snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs1554888939
rs1554888939
0.683 0.640 9 137798823 missense variant G/T snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs1057519389
rs1057519389
0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 1.000 1 2017 2017
dbSNP: rs1557043622
rs1557043622
0.695 0.400 X 48909843 missense variant C/A snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 1.000 1 2019 2019
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 1.000 1 2016 2016
dbSNP: rs1569548274
rs1569548274
0.701 0.520 X 154030553 splice acceptor variant TCCAGTGAGCCTCCTCTGGGCATCTTCTCCTCTTTGCAGACGCTGCTGCTCAAGTCCTGGGGCTCAGGGGGGCTGGTGGGGTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTGGCACGGGGGCCTTTGGGGACTCTGAGTGGTGGTGATGGTGGTGGTGCTCCTTCTTGGGGGGTGAGGAGGCGCTGCTGCTGCGCCCCTTGGGGCTGCTCTCCTTGCTTTTCCGCCCAGGGCTCTTACAGGTCTTCAGTCCTTTCCCGCTCTTCTCACCGAGGGTGGACACCAGCAGGGGCTTCACCACTTCCTTGACCTCGATGCTGACCGTCTCCCGGGTCTTGCGCTTCTTGATGGGGAGTACGGTCTCCTGCACAGATCGGATAGAAGACTCCTTCACGGCTTTCTTTTTGGCCTCGGCGGCAGCGGCTGCCACCACACTCCCCGGCTTTCGGCCCCGTTTCTTGGGAATGGCCTGAGGGTCGGCCTCAGCTTTTCGCTTCCTGCCGGGGCGTTTGATCACCATGACCTGGGTGGATGTGGTGGCCCCACCCCCCTCAGC/- delins
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs765379963
rs765379963
0.701 0.520 1 165743172 stop gained G/A snv 1.2E-05 2.1E-05
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs1569509136
rs1569509136
0.708 0.400 X 53647576 splice acceptor variant T/C snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs387907144
rs387907144
0.716 0.600 6 157181056 stop gained C/A;T snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 1.000 2 2012 2015
dbSNP: rs1085307993
rs1085307993
0.716 0.440 5 161331056 missense variant C/T snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs137854539
rs137854539
0.716 0.520 20 58903703 missense variant C/T snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs1555462347
rs1555462347
0.716 0.520 16 8901028 frameshift variant CT/- delins
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs1564045331
rs1564045331
XPA
0.716 0.320 9 97687208 inframe deletion ATTCTT/- delins
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs778543124
rs778543124
XPA
0.716 0.320 9 97675476 frameshift variant AGTCTTACGGTACA/- delins 6.8E-05 6.3E-05
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs121909574
rs121909574
0.724 0.400 6 10404509 missense variant T/A;C;G snv 4.6E-06
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 1.000 1 2015 2015
dbSNP: rs1564919048
rs1564919048
0.732 0.280 10 121520106 missense variant C/A snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs28934907
rs28934907
0.732 0.320 X 154032268 missense variant G/A;C snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs752746786
rs752746786
0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 1.000 1 2016 2016
dbSNP: rs34757931
rs34757931
0.742 0.360 11 119081189 missense variant T/G snv 1.2E-04 5.6E-05
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0