List of variants in gene BCL11B reported as uncertain significance for immune system disorder

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_138576.4(BCL11B):c.908C>A (p.Pro303Gln)	rs752385859	0.00003
NM_138576.4(BCL11B):c.1003A>G (p.Met335Val)	rs1886500576
NM_138576.4(BCL11B):c.1644C>A (p.Asn548Lys)
NM_138576.4(BCL11B):c.296C>T (p.Pro99Leu)	rs1889207328
NM_138576.4(BCL11B):c.307C>A (p.Arg103Ser)
NM_138576.4(BCL11B):c.740G>A (p.Arg247His)	rs748264333
NM_138576.4(BCL11B):c.906C>A (p.His302Gln)	rs1886508540
NM_138576.4(BCL11B):c.992G>T (p.Ser331Ile)

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