"Counsyl"[submitter] AND "MIR3936HG"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 556202	NM_003060.4(SLC22A5):c.-131A>C	LOC129994569, MIR3936HG +1 more	Single nucleotide variant (5 prime UTR variant)	Renal carnitine transport defect	GUncertain significance
Select item 556691	NM_003060.4(SLC22A5):c.-129_-102del	LOC129994569, MIR3936HG +1 more	Deletion (5 prime UTR variant)	Renal carnitine transport defect	GUncertain significance
Select item 25342	NM_003060.4(SLC22A5):c.-78C>T	LOC129994569, MIR3936HG +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +2 more	GBenign
Select item 25343	NM_003060.4(SLC22A5):c.-77G>A	LOC129994569, MIR3936HG +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +2 more	GBenign

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