List of variants in gene IMPG2 reported as likely benign for Retinitis pigmentosa

Minimum submission review status:		Collection method:
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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_016247.4(IMPG2):c.*1954G>A	rs113855688	0.02856
NM_016247.4(IMPG2):c.1908T>C (p.Asp636=)	rs35648234	0.02002
NM_016247.4(IMPG2):c.*1282C>T	rs116405398	0.01799
NM_016247.4(IMPG2):c.*444G>A	rs115229467	0.01734
NM_016247.4(IMPG2):c.*446G>A	rs115295966	0.01632
NM_016247.4(IMPG2):c.*1595G>A	rs59589993	0.01167
NM_016247.4(IMPG2):c.*3049G>A	rs112062476	0.01164
NM_016247.4(IMPG2):c.*260A>G	rs73863023	0.00919
NM_016247.4(IMPG2):c.*2885C>A	rs77671634	0.00918
NM_016247.4(IMPG2):c.*2869C>T	rs184922362	0.00638

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