List of variants in gene BCL11B reported as likely benign for immune system 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_138576.4(BCL11B):c.1521C>T (p.Gly507=)	rs745896590	0.00062
NM_138576.4(BCL11B):c.1996C>T (p.Pro666Ser)
NM_138576.4(BCL11B):c.2108C>A (p.Pro703Gln)
NM_138576.4(BCL11B):c.473C>T (p.Ala158Val)

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