"MAP6D1-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052530	NM_024871.4(MAP6D1):c.522C>T (p.Val174=)	MAP6D1	Single nucleotide variant (synonymous variant)	MAP6D1-related disorder	GLikely benign
Select item 3051491	NM_024871.4(MAP6D1):c.261G>A (p.Pro87=)	MAP6D1	Single nucleotide variant (synonymous variant)	MAP6D1-related disorder	GLikely benign
Select item 3035858	NM_024871.4(MAP6D1):c.237C>T (p.Pro79=)	LOC129938032, MAP6D1	Single nucleotide variant (synonymous variant)	MAP6D1-related disorder	GBenign

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