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601072.G
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Subject Details
Country
United Arab Emirates
HPO Terms
Congenital sensorineural hearing impairment
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Sex
Unknown
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_001256317.3:c.800C>A
4
Deafness, Autosomal Recessive 8
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Remarks
Autosomal recessive
References
Elsayed O and Al-Shamsi A. 2022
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