"HMGA2-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3033836	NM_003483.6(HMGA2):c.15T>G (p.Gly5=)	HMGA2	Single nucleotide variant (synonymous variant)	HMGA2-related disorder	GLikely benign
Select item 768565	NM_003483.6(HMGA2):c.199-8A>G	HMGA2	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 3044402	NM_003483.6(HMGA2):c.250-36267A>G	HMGA2 (K103E)	Single nucleotide variant (3 prime UTR variant +2 more)	HMGA2-related disorder	GBenign
Select item 3033396	NM_003483.6(HMGA2):c.250-36248T>C	HMGA2	Single nucleotide variant (3 prime UTR variant +1 more)	HMGA2-related disorder	GBenign
Select item 784302	NM_003483.6(HMGA2):c.274C>G (p.Pro92Ala)	HMGA2 (P92A)	Single nucleotide variant (missense variant)	HMGA2-related disorder +1 more	GBenign/Likely benign
Select item 3055904	NM_003483.6(HMGA2):c.282+1012T>C	HMGA2	Single nucleotide variant (synonymous variant +1 more)	HMGA2-related disorder	GBenign
Select item 3043910	NM_003483.6(HMGA2):c.*1G>A	HMGA2	Single nucleotide variant (3 prime UTR variant)	HMGA2-related disorder	GLikely benign

ClinVar