List of variants in gene GNB5 reported as benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_016194.4(GNB5):c.312C>T (p.His104=)	rs6493537	0.11749
NM_016194.4(GNB5):c.936A>G (p.Ala312=)	rs34059787	0.03765
NM_016194.4(GNB5):c.567G>A (p.Lys189=)	rs17612637	0.02649
NM_016194.4(GNB5):c.252G>A (p.Ala84=)	rs35581121	0.02626
NM_016194.4(GNB5):c.638C>T (p.Ala213Val)	rs34637551	0.01003
NM_016194.4(GNB5):c.1107C>T (p.Arg369=)	rs113335851	0.00486
NM_016194.4(GNB5):c.239-9383C>T	rs59987655
NM_016194.4(GNB5):c.239-9436T>C	rs28835411

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