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612712.3
Home
Subject Details
Country
Saudi Arabia
HPO Terms
Retinal dystrophy
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Sex
Female
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_152443.3:c.139G>A
2
Leber Congenital Amaurosis 13
Download Table
References
Monies et al. 2017
Related Subjects
Subject Id
Country
HPO Terms
Sex
Family History
Parental Consanguinity
Remarks
612712.2
Saudi Arabia
Rod-cone dystrophy
Unknown
No
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