List of variants in gene PRPH2 reported as likely pathogenic for Vitelliform macular dystrophy 2

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000322.5(PRPH2):c.628C>T (p.Pro210Ser)	rs61755797
NM_000322.5(PRPH2):c.635G>C (p.Ser212Thr)	rs61755801
NM_000322.5(PRPH2):c.903_906del (p.Ser301fs)	rs1799988458

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