rs104894470
|
GPHN;RDH12
|
Leber Congenital Amaurosis
|
|
0.010 |
GeneticVariation |
BEFREE |
The retinal disease in persons with RDH12 mutations in the homozygous (p.G127X, p.Q189X, p.Y226C, p.A269GfsX1, and p.L274P) or compound heterozygous state (p.R65X/p.A269GfsX1, p.H151D/p.T155I, p.H151D/p.A269GfsX1) was diagnosed initially as Leber congenital amaurosis (LCA) or early-onset retinitis pigmentosa.
|
17389517 |
2007 |
rs104894474
|
GPHN;RDH12
|
Leber Congenital Amaurosis
|
|
0.010 |
GeneticVariation |
BEFREE |
The retinal disease in persons with RDH12 mutations in the homozygous (p.G127X, p.Q189X, p.Y226C, p.A269GfsX1, and p.L274P) or compound heterozygous state (p.R65X/p.A269GfsX1, p.H151D/p.T155I, p.H151D/p.A269GfsX1) was diagnosed initially as Leber congenital amaurosis (LCA) or early-onset retinitis pigmentosa.
|
17389517 |
2007 |
rs17852293
|
GPHN;RDH12
|
Amaurosis congenita of Leber, type 1
|
|
0.010 |
GeneticVariation |
BEFREE |
A novel compound heterozygote T49M/A269fsX270 mutation was also found in a patient with LCA, and both homozygous and heterozygous R161Q changes were seen in 26 patients affected with LCA, CORD or RP.
|
17512964 |
2007 |
rs373032226
|
GPHN;RDH12
|
Amaurosis congenita of Leber, type 1
|
|
0.010 |
GeneticVariation |
BEFREE |
Of the six changes identified, three were novel including a homozygous C201R change in a patient affected with LCA, a heterozygous A177V change in patients affected with CORD and a heterozygous G46G change in a patient affected with LCA.
|
17512964 |
2007 |
rs373032226
|
GPHN;RDH12
|
Cone-Rod Dystrophy 2
|
|
0.010 |
GeneticVariation |
BEFREE |
Of the six changes identified, three were novel including a homozygous C201R change in a patient affected with LCA, a heterozygous A177V change in patients affected with CORD and a heterozygous G46G change in a patient affected with LCA.
|
17512964 |
2007 |
rs104894472
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs104894473
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs104894475
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs104894475
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs104894476
|
GPHN;ZFYVE26;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs28940313
|
GPHN;ZFYVE26;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
G |
0.800 |
GeneticVariation |
CLINVAR |
|
|
|
rs28940313
|
GPHN;ZFYVE26;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs28940314
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs28940315
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
A |
0.800 |
CausalMutation |
CLINVAR |
RDH12 retinopathy: novel mutations and phenotypic description.
|
22065924 |
2011 |
rs28940315
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
A |
0.800 |
CausalMutation |
CLINVAR |
Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosis.
|
15322982 |
2004 |
rs28940315
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
A |
0.800 |
CausalMutation |
CLINVAR |
Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mapping.
|
24474277 |
2014 |
rs28940315
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
A |
0.800 |
CausalMutation |
CLINVAR |
Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies.
|
26306921 |
2015 |
rs104894470
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs104894471
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
T |
0.700 |
CausalMutation |
CLINVAR |
Molecular Screening of 43 Brazilian Families Diagnosed with Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy.
|
29186038 |
2017 |
rs104894471
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
T |
0.700 |
CausalMutation |
CLINVAR |
Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa.
|
26497376 |
2015 |
rs104894471
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy.
|
15258582 |
2004 |
rs104894471
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
T |
0.700 |
CausalMutation |
CLINVAR |
Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosis.
|
15322982 |
2004 |
rs104894474
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
T |
0.700 |
CausalMutation |
CLINVAR |
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies.
|
26355662 |
2016 |
rs104894474
|
GPHN;RDH12
|
Retinitis Pigmentosa
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
|
30718709 |
2019 |
rs104894474
|
GPHN;RDH12
|
LEBER CONGENITAL AMAUROSIS 13
|
T |
0.700 |
CausalMutation |
CLINVAR |
Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosis.
|
15322982 |
2004 |