List of variants in gene BICD2 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001003800.2(BICD2):c.1438G>A (p.Ala480Thr)	rs140188204	0.00011
NM_001003800.2(BICD2):c.1376C>T (p.Thr459Met)	rs777065935	0.00001
NM_001003800.2(BICD2):c.1063A>T (p.Met355Leu)	rs767226677
NM_001003800.2(BICD2):c.527G>A (p.Arg176His)	rs1207286970
NM_001003800.2(BICD2):c.754G>A (p.Glu252Lys)	rs776953074

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