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

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

Download table as spreadsheet

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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.