List of variants in gene P2RX2 reported as benign for perceptual disorders

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_170682.4(P2RX2):c.468T>C (p.Thr156=)	rs7964634	0.67274
NM_170682.4(P2RX2):c.636-13G>A	rs6560891	0.66828
NM_170682.4(P2RX2):c.997-40C>T	rs4883632	0.53086
NM_170682.4(P2RX2):c.173+28_173+41del	rs200710959

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