List of variants in gene BICRA reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001394372.1(BICRA):c.1225G>T (p.Val409Leu)	rs1444702735
NM_001394372.1(BICRA):c.1958C>A (p.Pro653Gln)	rs2514111796
NM_001394372.1(BICRA):c.3313C>T (p.Pro1105Ser)

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