"PreventionGenetics, part of Exact Sciences"[submitter] AND "PRH1-PRR4 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042965	NM_007244.3(PRR4):c.*18+3A>C	PRH1-PRR4, PRR4	Single nucleotide variant (intron variant)	PRR4-related disorder	GLikely benign
Select item 3060347	NM_007244.3(PRR4):c.359A>G (p.Gln120Arg)	PRH1-PRR4, PRR4 (Q120R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	PRR4-related disorder	GBenign
Select item 3060846	NM_007244.3(PRR4):c.287G>A (p.Arg96Gln)	PRH1-PRR4, PRR4 (R96Q)	Single nucleotide variant (non-coding transcript variant +2 more)	PRR4-related disorder	GBenign

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