List of variants in gene P2RX2 reported as likely benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_170682.4(P2RX2):c.-10C>T	rs566193497	0.00167
NM_170682.4(P2RX2):c.211G>A (p.Glu71Lys)	rs143664462	0.00163
NM_170682.4(P2RX2):c.491A>G (p.Gln164Arg)	rs142844880	0.00097
NM_170682.4(P2RX2):c.922A>G (p.Lys308Glu)	rs115331525	0.00051
NM_170682.4(P2RX2):c.1176T>C (p.Pro392=)	rs189869132	0.00044
NM_170682.4(P2RX2):c.1363G>A (p.Glu455Lys)	rs199955493	0.00020
NM_170682.4(P2RX2):c.762G>A (p.Glu254=)	rs144300117	0.00013
NM_170682.4(P2RX2):c.1219G>A (p.Gly407Ser)	rs199712315	0.00008
NM_170682.4(P2RX2):c.1310G>A (p.Arg437Gln)	rs115260724	0.00003
NM_170682.4(P2RX2):c.1413C>T (p.Leu471=)	rs568364905	0.00001
NM_170682.4(P2RX2):c.1257A>C (p.Ser419=)	rs876657561
NM_170682.4(P2RX2):c.1295C>G (p.Ala432Gly)
NM_170682.4(P2RX2):c.309+11C>T
NM_170682.4(P2RX2):c.457+9G>A	rs200457240
NM_170682.4(P2RX2):c.774+9A>C	rs373022527

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