List of variants in gene LMAN1 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_005570.4(LMAN1):c.*2929T>C	rs4806	0.27360
NM_005570.4(LMAN1):c.351A>G (p.Arg117=)	rs1127220	0.23450
NM_005570.4(LMAN1):c.*2217G>A	rs7236294	0.11367
NM_005570.4(LMAN1):c.1228A>T (p.Met410Leu)	rs2298711	0.10604
NM_005570.4(LMAN1):c.*2387A>G	rs34679996	0.10136
NM_005570.4(LMAN1):c.*1799A>C	rs1043334	0.09774
NM_005570.4(LMAN1):c.*2063C>G	rs7239187	0.08931
NM_005570.4(LMAN1):c.*2405C>A	rs34753206	0.05461
NM_005570.4(LMAN1):c.*2184A>G	rs41370447	0.01057
NM_005570.4(LMAN1):c.957G>A (p.Ala319=)	rs61733371	0.00861
NM_005570.4(LMAN1):c.*1822G>T	rs151128517	0.00725
NM_005570.4(LMAN1):c.*3107T>A	rs3760558	0.00267
NM_005570.4(LMAN1):c.*490C>T	rs117480907	0.00265
NM_005570.4(LMAN1):c.*1493A>G	rs529247031	0.00029

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