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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASPHD1, KCTD13
Single nucleotide variant
(synonymous variant +1 more)
KCTD13-related disorder
GLikely benign
KCTD13
Single nucleotide variant
(synonymous variant +1 more)
KCTD13-related disorder
GLikely benign
KCTD13, LOC130058798
Single nucleotide variant
(5 prime UTR variant +1 more)
KCTD13-related disorder
GLikely benign
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