List of variants in gene GNB3 reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_002075.4(GNB3):c.657T>A (p.Arg219=)	rs45476395	0.00653
NM_002075.4(GNB3):c.401A>G (p.Lys134Arg)	rs61747607	0.00219
NM_002075.4(GNB3):c.81C>T (p.Asp27=)	rs145085793	0.00202
NM_002075.4(GNB3):c.699+18C>A	rs199571092	0.00071
NM_002075.4(GNB3):c.141G>A (p.Thr47=)	rs149095347	0.00027
NM_002075.4(GNB3):c.203+11G>C	rs373777248
NM_002075.4(GNB3):c.203+16del	rs545677946
NM_002075.4(GNB3):c.699+115A>C	rs11064426
NM_002075.4(GNB3):c.699+139_699+141del	rs34871066
NM_002075.4(GNB3):c.699+140_699+141del	rs34871066
NM_002075.4(GNB3):c.699+141del	rs34871066
NM_002075.4(GNB3):c.699+141dup	rs34871066
NM_002075.4(GNB3):c.699+15del	rs1565519172
NM_002075.4(GNB3):c.699+15dup	rs1565519172
NM_002075.4(GNB3):c.96+11dup	rs1555123399

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