LOC126862154[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154848	GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	LOC130057816, LOC130057817 +1763 more	Copy number gain	See cases	GPathogenic
Select item 2219755	NM_015920.4(RPS27L):c.89C>T (p.Ser30Phe)	LOC126862154, RPS27L (S30F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance