List of variants in gene combination BCL10, LOC126805771 reported as likely benign for Immunodeficiency 37

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_003921.5(BCL10):c.57+13G>A	rs199588735	0.00011
NM_003921.5(BCL10):c.57+9C>T	rs369858521	0.00007
NM_003921.5(BCL10):c.6G>A (p.Glu2=)	rs200626032	0.00004
NM_003921.5(BCL10):c.12C>T (p.Thr4=)	rs1292365915	0.00002
NM_003921.5(BCL10):c.27C>T (p.Thr9=)	rs779616837	0.00001
NM_003921.5(BCL10):c.33G>A (p.Glu11=)	rs755937538	0.00001
NM_003921.5(BCL10):c.54G>A (p.Lys18=)	rs757265980	0.00001
NM_003921.5(BCL10):c.36C>T (p.Asp12=)
NM_003921.5(BCL10):c.42T>A (p.Thr14=)	rs1570341297
NM_003921.5(BCL10):c.42T>G (p.Thr14=)
NM_003921.5(BCL10):c.57+16G>A	rs2527119569

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