List of variants in gene MTTP reported as uncertain significance for overnutrition

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001386140.1(MTTP):c.1301C>T (p.Thr434Ile)	rs1467372840	0.00015
NM_001386140.1(MTTP):c.1636A>G (p.Ile546Val)	rs200992175	0.00001
NM_001386140.1(MTTP):c.863C>A (p.Pro288His)	rs1022457887	0.00001
NM_001386140.1(MTTP):c.1385A>T (p.Glu462Val)	rs757598679

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