List of variants in gene GNB1 reported as likely benign for hematologic disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002074.5(GNB1):c.462C>T (p.Asp154=)	rs77027087	0.01689
NM_002074.5(GNB1):c.402C>T (p.Arg134=)	rs560214051	0.00011

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