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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EIF1B-AS1, MYRIP
(P137L +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign/Likely benign
EIF1B-AS1, MYRIP
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign/Likely benign