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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FDXR
(R392W +6 more)
Single nucleotide variant
(missense variant +1 more)
Auditory neuropathy-optic atrophy syndrome
+2 more
GPathogenic/Likely pathogenic
FDXR
(R176W +6 more)
Single nucleotide variant
(missense variant +1 more)
Auditory neuropathy-optic atrophy syndrome
GUncertain significance
FDXR
(I167F +6 more)
Single nucleotide variant
(missense variant +1 more)
Auditory neuropathy-optic atrophy syndrome
GLikely pathogenic
FDXR
(V150M +5 more)
Single nucleotide variant
(missense variant +1 more)
Auditory neuropathy-optic atrophy syndrome
GLikely pathogenic
BTBD17, ARMC7
+40 more
Copy number gain
not provided
GPathogenic
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