"Ambry Genetics"[submitter] AND "LOC129998186"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259949	NM_147128.4(ZNRF2):c.19G>A (p.Gly7Ser)	LOC105375218, LOC129998186 +1 more (G7S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199178	NM_147128.4(ZNRF2):c.44C>T (p.Thr15Met)	LOC105375218, LOC129998186 +1 more (T15M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance