List of variants in gene BCL9L reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001378213.1(BCL9L):c.4182T>C (p.Pro1394=)	rs7104819	0.49499
NM_001378213.1(BCL9L):c.4020G>A (p.Gln1340=)	rs61751532	0.05636
NM_001378213.1(BCL9L):c.2292C>T (p.Pro764=)	rs61730467	0.03592
NM_001378213.1(BCL9L):c.1627A>G (p.Ser543Gly)	rs78780803	0.02211
NM_001378213.1(BCL9L):c.1272C>T (p.Ser424=)	rs75656086	0.01556
NM_001378213.1(BCL9L):c.2705T>C (p.Val902Ala)	rs34123504	0.01152
NM_001378213.1(BCL9L):c.1936A>G (p.Met646Val)	rs34752197	0.01150

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