"Fulgent Genetics, Fulgent Genetics"[submitter] AND "POT1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 475044	NM_015450.3(POT1):c.1416T>G (p.Ser472Arg)	POT1 (S472R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 541870	NM_015450.3(POT1):c.1183G>A (p.Gly395Ser)	POT1 (G395S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity