List of variants in gene combination MMAB, MVK reported as benign for disorder of metabolite absorption and transport

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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_052845.4(MMAB):c.57C>A (p.Arg19=)	rs10774774	0.31358
NM_052845.4(MMAB):c.56G>A (p.Arg19His)	rs10774775	0.31347
NM_052845.4(MMAB):c.288T>C (p.Ile96=)	rs62000414	0.04206
NC_000012.12:g.109573660G>A	rs66486014	0.00733
NM_052845.4(MMAB):c.185C>T (p.Thr62Met)	rs115802744	0.00177
NM_052845.4(MMAB):c.10T>C (p.Cys4Arg)	rs146668962	0.00104
NM_052845.4(MMAB):c.-9G>T	rs554831769
NM_052845.4(MMAB):c.56_57delinsAA (p.Arg19Gln)	rs36013132

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