List of variants in gene PRPH2 reported as likely benign for not provided

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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_000322.5(PRPH2):c.1013A>G (p.Asp338Gly)	rs434102	0.77412
NM_000322.5(PRPH2):c.133C>T (p.Leu45Phe)	rs61755770	0.00414
NM_000322.5(PRPH2):c.866C>T (p.Ser289Leu)	rs62645939	0.00079
NM_000322.5(PRPH2):c.249C>T (p.Tyr83=)	rs61755775	0.00053
NM_000322.5(PRPH2):c.909C>T (p.Ser303=)	rs144111167	0.00049
NM_000322.5(PRPH2):c.938C>T (p.Pro313Leu)	rs61748434	0.00044
NM_000322.5(PRPH2):c.264A>C (p.Pro88=)	rs1294407459	0.00034
NM_000322.5(PRPH2):c.37C>T (p.Arg13Trp)	rs61754402	0.00018
NM_000322.5(PRPH2):c.252C>T (p.Asp84=)	rs139936445	0.00017
NM_000322.5(PRPH2):c.300G>A (p.Pro100=)	rs150695654	0.00011
NM_000322.5(PRPH2):c.801C>T (p.Val267=)	rs189358082	0.00002
NM_000322.5(PRPH2):c.205G>T (p.Val69Leu)	rs558060514	0.00001
NM_000322.5(PRPH2):c.*484dup	rs55851577
NM_000322.5(PRPH2):c.387C>T (p.Thr129=)	rs1582780697
NM_000322.5(PRPH2):c.483C>G (p.Ile161Met)	rs76989855

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