"GeneDx"[submitter] AND "ATRNL1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1320613	NM_207303.4(ATRNL1):c.2966G>A (p.Ser989Asn)	ATRNL1 (S989N)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1676870	NM_207303.4(ATRNL1):c.3609A>G (p.Thr1203=)	ATRNL1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 253479	GRCh37/hg19 10q24.32-26.3(chr10:103288313-135512075)x3	ABLIM1, ABRAXAS2 +201 more	Copy number gain	See cases	GPathogenic

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