List of variants in gene MMAB reported as likely benign by Illumina Laboratory Services, Illumina

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_052845.4(MMAB):c.*1409G>A	rs72650177	0.05424
NM_052845.4(MMAB):c.*368T>A	rs773284148	0.05387
NM_052845.4(MMAB):c.*2186T>C	rs147647465	0.00246
NM_052845.4(MMAB):c.*404T>G	rs148289390	0.00240
NM_052845.4(MMAB):c.*1859TA[7]	rs10623308
NM_052845.4(MMAB):c.*1859TA[9]	rs10623308

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