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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130064867, RPL18
Single nucleotide variant
(5 prime UTR variant +1 more)
RPL18-related disorder
GLikely benign
LOC130064867, RPL18
Single nucleotide variant
(intron variant)
not provided
GBenign