"Ambry Genetics"[submitter] AND "GNRH2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3281821	NM_178331.2(GNRH2):c.5C>T (p.Ala2Val)	GNRH2 (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321926	NM_178331.2(GNRH2):c.53T>C (p.Leu18Pro)	GNRH2 (L18P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3281822	NM_178331.2(GNRH2):c.112C>T (p.Leu38Phe)	GNRH2 (L38F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412103	NM_178331.2(GNRH2):c.241A>G (p.Thr81Ala)	GNRH2 (T81A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462953	NM_178331.2(GNRH2):c.242C>T (p.Thr81Met)	GNRH2 (T81M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2404142	NM_178331.2(GNRH2):c.292A>G (p.Thr98Ala)	GNRH2 (T98A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100698	NM_178331.2(GNRH2):c.304G>A (p.Glu102Lys)	GNRH2, LOC130065317 (E102K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348666	NM_178331.2(GNRH2):c.305A>C (p.Glu102Ala)	GNRH2, LOC130065317 (E101A +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

ClinVar