Related gene-specific medical variations for Gene (Select 3176) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2502178	NM_006895.3(HNMT):c.137+2287G>A	HNMT	Single nucleotide variant (intron variant)	Inherited susceptibility to asthma +1 more	GUncertain significance
Select item 2432492	NM_006895.3(HNMT):c.534C>T (p.Gly178=)	HNMT	Single nucleotide variant (synonymous variant)	Intellectual disability, autosomal recessive 51	GUncertain significance
Select item 687455	GRCh37/hg19 2q22.1(chr2:138673890-138792148)x3	HNMT	Copy number gain	not provided	GUncertain significance

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