List of variants in gene combination LOC126806368, MMADHC reported as benign for hematologic disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_015702.3(MMADHC):c.-49T>C	rs79997772	0.02222
NM_015702.3(MMADHC):c.9+14C>T	rs140075619	0.00140

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