List of variants in gene combination LOC126806368, MMADHC, MMADHC-DT 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_015702.3(MMADHC):c.-60G>A	rs886054923	0.00013
NM_015702.3(MMADHC):c.-136G>C	rs1682898571
NM_015702.3(MMADHC):c.-62G>A	rs886054924

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