Variants in gene PRPH2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_000322.5(PRPH2):c.929G>A (p.Arg310Lys)	rs425876	0.92861
NM_000322.5(PRPH2):c.910C>G (p.Gln304Glu)	rs390659	0.78498
NM_000322.5(PRPH2):c.1013A>G (p.Asp338Gly)	rs434102	0.77412
NM_000322.5(PRPH2):c.318T>C (p.Val106=)	rs7764439	0.59853
NM_000322.5(PRPH2):c.582-67T>A	rs3818086	0.56178
NM_000322.5(PRPH2):c.582-85G>A	rs34722725	0.25301
NM_000322.5(PRPH2):c.829-48C>T	rs41273820	0.22114
NM_000322.5(PRPH2):c.133C>T (p.Leu45Phe)	rs61755770	0.00414
NM_000322.5(PRPH2):c.249C>T (p.Tyr83=)	rs61755775	0.00053
NM_000322.5(PRPH2):c.*484del	rs55851577

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