Related gene-specific medical variations for Gene (Select 25802) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065391	NM_012134.3(LMOD1):c.139G>A (p.Val47Met)	LMOD1 (V47M)	Single nucleotide variant (missense variant)	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3	GUncertain significance
Select item 3064415	NM_012134.3(LMOD1):c.1433G>A (p.Arg478Gln)	LMOD1 (R478Q)	Single nucleotide variant (missense variant)	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3	GUncertain significance