List of variants in gene CACNB4 reported as benign for not provided

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000726.5(CACNB4):c.64-58C>G	rs34347895	0.15912
NM_000726.5(CACNB4):c.762T>A (p.Ile254=)	rs61736804	0.05586
NM_000726.5(CACNB4):c.1303-3T>C	rs143442080	0.00617
NM_000726.5(CACNB4):c.*624A>T	rs755272601	0.00332
NM_000726.5(CACNB4):c.*1942T>C	rs139629003	0.00300
NM_000726.5(CACNB4):c.*5022A>G	rs548177540	0.00298
NM_000726.5(CACNB4):c.1413G>A (p.Arg471=)	rs1805029	0.00148
NM_000726.5(CACNB4):c.*2188T>G	rs548234328	0.00122
NM_000726.5(CACNB4):c.*1814G>A	rs181447432	0.00103
NM_000726.5(CACNB4):c.*737C>T	rs558590558	0.00096
NM_000726.5(CACNB4):c.311G>T (p.Cys104Phe)	rs1805031	0.00074
NM_000726.5(CACNB4):c.147+13G>A	rs557705317	0.00003
NM_000726.5(CACNB4):c.288C>T (p.Ala96=)	rs558998873	0.00001
NM_000726.5(CACNB4):c.699+239C>T

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