rs61751374
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
|
30718709 |
2019 |
rs62645944
|
|
A |
0.710 |
GeneticVariation |
CLINVAR |
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
|
30718709 |
2019 |
rs1800552
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
|
30718709 |
2019 |
rs1800728
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
|
30718709 |
2019 |
rs201471607
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
|
30718709 |
2019 |
rs41292677
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
|
30718709 |
2019 |
rs61751392
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
|
30718709 |
2019 |
rs76157638
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
|
30718709 |
2019 |
rs779466403
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
|
30718709 |
2019 |
rs1553192726
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical and molecular characteristics of childhood-onset Stargardt disease.
|
25312043 |
2015 |
rs863223338
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa.
|
26497376 |
2015 |
rs749526785
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Homozygosity mapping in patients with cone-rod dystrophy: novel mutations and clinical characterizations.
|
20554613 |
2010 |
rs281865377
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.
|
11527935 |
2001 |
rs61749451
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1).
|
11594993 |
2001 |
rs61751399
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease.
|
9973280 |
1999 |
rs61751392
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies.
|
9781034 |
1998 |
rs1064793013
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1553188588
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs61750639
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs61753030
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs76157638
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|