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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LFNG
Single nucleotide variant
(synonymous variant +1 more)
Spondylocostal dysostosis 3, autosomal recessive
GLikely benign
LFNG
(R231C +2 more)
Single nucleotide variant
(missense variant +1 more)
Spondylocostal dysostosis 3, autosomal recessive
GUncertain significance