List of variants in gene CACNB2 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_201596.3(CACNB2):c.993G>A (p.Ser331=)	rs76956014	0.00852
NM_201596.3(CACNB2):c.1488+13_1488+33dup	rs757040188	0.00361
NM_201596.3(CACNB2):c.641G>C (p.Ser214Thr)	rs149253719	0.00078
NM_201596.3(CACNB2):c.590C>T (p.Ser197Phe)	rs150528041	0.00064
NM_201596.3(CACNB2):c.*835AAGT[3]	rs547804393
NM_201596.3(CACNB2):c.121-3_121-2insTGT	rs769211879
NM_201596.3(CACNB2):c.121-3_121-2insTTTTTTTTTTTTTTTTTTTTTTTTTTT

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