ClinVar Miner

List of variants in gene combination AIFM1, RAB33A reported as likely benign for X-linked hereditary sensory and autonomic neuropathy with deafness

Included ClinVar conditions (2):
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Gene type:
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Total variants: 1
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NM_004208.4(AIFM1):c.1113C>T (p.Ser371=) rs724160027

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