C3540453[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 4794	NM_181882.3(PRX):c.3208C>T (p.Arg1070Ter)	PRX (R1070*)	Single nucleotide variant (3 prime UTR variant +1 more)	Charcot-Marie-Tooth disease type 4 +2 more	GPathogenic/Likely pathogenic
Select item 1687279	NM_181882.3(PRX):c.3098del (p.Thr1033fs)	PRX (T1033fs)	Deletion (3 prime UTR variant +1 more)	Charcot-Marie-Tooth disease type 4 +1 more	GPathogenic/Likely pathogenic