List of variants in gene P2RX2 reported as 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: 16

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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.-36T>C	rs7314492	0.08839
NM_170682.4(P2RX2):c.9C>T (p.Ala3=)	rs186684886	0.02469
NM_170682.4(P2RX2):c.554+14C>A	rs151253585	0.01337
NM_170682.4(P2RX2):c.1302G>A (p.Pro434=)	rs114276183	0.01262
NM_170682.4(P2RX2):c.186C>T (p.Ile62=)	rs75585377	0.01034
NM_170682.4(P2RX2):c.174-4G>T	rs200811971	0.00818
NM_170682.4(P2RX2):c.699C>T (p.Asp233=)	rs113782309	0.00585
NM_170682.4(P2RX2):c.1332T>A (p.Pro444=)	rs116834114	0.00302
NM_170682.4(P2RX2):c.831G>A (p.Ser277=)	rs114365804	0.00190
NM_170682.4(P2RX2):c.774+7C>G	rs199743808	0.00186
NM_170682.4(P2RX2):c.491A>G (p.Gln164Arg)	rs142844880	0.00097
NM_170682.4(P2RX2):c.964G>A (p.Gly322Arg)	rs201474543	0.00008
NM_170682.4(P2RX2):c.1325_1335del (p.Ile441_Ser442insTer)	rs876657423
NM_170682.4(P2RX2):c.775-8_775-6del	rs876657424

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