List of variants in gene LMAN1 reported as likely benign for coagulation protein disease

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005570.4(LMAN1):c.*164A>G	rs41332251	0.00758
NM_005570.4(LMAN1):c.936C>T (p.Pro312=)	rs145829103	0.00609
NM_005570.4(LMAN1):c.*1921T>C	rs74735102	0.00327
NM_005570.4(LMAN1):c.821C>T (p.Pro274Leu)	rs41476148	0.00241
NM_005570.4(LMAN1):c.214+7C>T	rs2277728	0.00080
NM_005570.4(LMAN1):c.*860T>G	rs41331148
NM_005570.4(LMAN1):c.539+5GT[3]	rs3835325

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