List of variants in gene combination LOC126807124, MTTP reported as uncertain significance for anemia

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_000253.3(MTTP):c.-214G>A	rs569667113	0.00066
NM_000253.4(MTTP):c.-153C>G	rs886058954	0.00004
NM_000253.4(MTTP):c.-205G>A	rs886058953	0.00001
NM_000253.4(MTTP):c.-149C>A	rs886058955

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