List of variants in gene NBEAL2 reported as uncertain significance by Birmingham Platelet Group; University of Birmingham

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_015175.3(NBEAL2):c.6866G>A (p.Arg2289Gln)	rs181413143	0.00289
NM_015175.3(NBEAL2):c.5021G>A (p.Arg1674His)	rs200622688	0.00088
NM_015175.3(NBEAL2):c.2375G>A (p.Arg792Gln)	rs140354422	0.00061
NM_015175.3(NBEAL2):c.5866G>A (p.Val1956Met)	rs373495718	0.00004
NM_015175.3(NBEAL2):c.3184G>A (p.Val1062Ile)	rs775313250	0.00003

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