"Eurofins Ntd Llc (ga)"[submitter] AND "P2RX2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 226984	NM_170682.4(P2RX2):c.468T>C (p.Thr156=)	P2RX2	Single nucleotide variant (synonymous variant +1 more)	Autosomal dominant nonsyndromic hearing loss 41 +2 more	GBenign
Select item 501253	NM_170682.4(P2RX2):c.491A>G (p.Gln164Arg)	P2RX2 (Q164R +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 226985	NM_170682.4(P2RX2):c.554+14C>A	P2RX2	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 226990	NM_170682.4(P2RX2):c.831G>A (p.Ser277=)	P2RX2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 514244	NM_170682.4(P2RX2):c.922A>G (p.Lys308Glu)	P2RX2 (K236E +4 more)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 501580	NM_170682.4(P2RX2):c.947C>T (p.Thr316Met)	P2RX2 (T244M +4 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity

ClinVar