List of variants in gene MCFD2 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_139279.6(MCFD2):c.*1267G>T	rs7596245	0.76204
NM_139279.6(MCFD2):c.*1752T>C	rs6544935	0.73719
NM_139279.6(MCFD2):c.*2454C>A	rs1051317	0.20979
NM_139279.6(MCFD2):c.*693G>C	rs28516550	0.11926
NM_139279.6(MCFD2):c.*2075C>T	rs6743966	0.11844
NM_139279.6(MCFD2):c.*2658C>T	rs17035887	0.11807
NM_139279.6(MCFD2):c.*498A>G	rs144674773	0.06645
NM_139279.6(MCFD2):c.*1908G>C	rs6743994	0.06473
NM_139279.6(MCFD2):c.*1924T>C	rs6715391	0.06423
NM_139279.6(MCFD2):c.*1525C>G	rs7596198	0.06380
NM_139279.6(MCFD2):c.*2675C>G	rs17035884	0.06201
NM_139279.6(MCFD2):c.*3318T>C	rs8861	0.05885
NM_139279.6(MCFD2):c.*133A>T	rs75416242	0.05300
NM_139279.6(MCFD2):c.*73A>G	rs71423925	0.04579
NM_139279.6(MCFD2):c.*3100C>G	rs13424086	0.03363
NM_139279.6(MCFD2):c.*1788C>T	rs115043642	0.03146
NM_139279.6(MCFD2):c.*1042C>T	rs111603188	0.02828
NM_139279.6(MCFD2):c.*1346G>T	rs111535939	0.02827
NM_139279.6(MCFD2):c.*2163A>G	rs140937815	0.02097
NM_139279.6(MCFD2):c.*1010G>T	rs138758588	0.01819
NM_139279.6(MCFD2):c.*1724C>T	rs115137793	0.01078
NM_139279.6(MCFD2):c.*1043G>A	rs114662283	0.01064
NM_139279.6(MCFD2):c.*2336A>C	rs144118640	0.01059
NM_139279.6(MCFD2):c.*1124G>A	rs190398265	0.01009
NM_139279.6(MCFD2):c.*1677T>G	rs28770495

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