List of variants in gene combination SNX17, ZNF513 reported as uncertain significance for Retinitis pigmentosa

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_144631.6(ZNF513):c.*29C>T	rs148848066	0.00062
NM_144631.6(ZNF513):c.*129G>A	rs560324766	0.00051
NM_144631.6(ZNF513):c.*134A>G	rs754539683	0.00028
NM_144631.6(ZNF513):c.*174G>A	rs558608689	0.00021
NM_144631.6(ZNF513):c.*15C>T	rs377145066	0.00020
NM_144631.6(ZNF513):c.*54C>T	rs149692692	0.00015
NM_144631.6(ZNF513):c.*225G>A	rs575633762	0.00013
NM_144631.6(ZNF513):c.*60C>T	rs753288919	0.00012
NM_144631.6(ZNF513):c.*254T>A	rs916987949	0.00001
NM_144631.6(ZNF513):c.*164G>A	rs1004503387
NM_144631.6(ZNF513):c.*217G>C	rs536704518

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