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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCD3
(G41E)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
ABCD3
(R117C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ABCD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ABCD3
Single nucleotide variant
(synonymous variant)
not provided
GBenign/Likely benign
ABCD3
(F461Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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