List of variants in gene combination LOC126806368, MMADHC reported as likely benign 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_015702.3(MMADHC):c.-8C>T	rs180812156	0.00282
NM_015702.3(MMADHC):c.9+12A>C	rs570608507	0.00001
NM_015702.3(MMADHC):c.9+12A>T
NM_015702.3(MMADHC):c.9+16C>T
NM_015702.3(MMADHC):c.9+17T>A	rs372601477
NM_015702.3(MMADHC):c.9+17T>G
NM_015702.3(MMADHC):c.9+18T>G	rs2105053453
NM_015702.3(MMADHC):c.9+19A>C

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