Related gene-specific medical variations for Gene (Select 4642) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3163427	NM_015194.3(MYO1D):c.16A>G (p.Ser6Gly)	MYO1D, MYO1D-DT (S6G)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 1526575	GRCh37/hg19 17q11.2(chr17:30888786-31207047)	MYO1D	Copy number loss	not specified	GUncertain significance
Select item 564428	GRCh37/hg19 17q11.2(chr17:30980351-31069557)x1	MYO1D	Copy number loss	not provided	GUncertain significance
Select item 157379	NM_015194.3(MYO1D):c.2865-44956_2865-37036del	MYO1D	Deletion (intron variant)	Preeclampsia	Gnot provided

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