276902.5.3

Country

Lebanon

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_174878.3:c.188A>C1

Remarks

Mother of 276902.5.1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
276902.5.1LebanonRod-cone dystrophy; Sensorineural hearing impairmentFemaleNoNo
276902.5.2LebanonMaleFather of 276902.5.1
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