List of variants in gene CD46 reported as benign for hematologic disorder

Minimum submission review status:		Collection method:
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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_172351.3(CD46):c.*897T>C	rs7144	0.40706
NM_172351.3(CD46):c.*1875T>G	rs1237	0.04298
NM_172351.3(CD46):c.*1435T>C	rs14374	0.03161
NM_172351.3(CD46):c.1083-10C>T	rs41317997	0.02234
NM_172351.3(CD46):c.*503A>G	rs2724390	0.02021
NM_172351.3(CD46):c.1013C>T (p.Ala338Val)	rs35366573	0.01505
NM_172351.3(CD46):c.*918G>A	rs6664092	0.01233
NM_172351.3(CD46):c.417A>G (p.Leu139=)	rs12126088	0.00583
NM_172351.3(CD46):c.453C>T (p.Ser151=)	rs145041158	0.00408
NM_172351.3(CD46):c.*1498G>T	rs117431447	0.00133

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