"Ambry Genetics"[submitter] AND "LOC130059913"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2403085	NM_006497.4(HIC1):c.512C>G (p.Pro171Arg)	HIC1, LOC130059913 (P171R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326206	NM_006497.4(HIC1):c.545C>G (p.Ala182Gly)	HIC1, LOC130059913 (A182G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance