List of variants in gene BSG reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001728.4(BSG):c.87G>A (p.Pro29=)	rs181004617	0.00043
NM_001728.4(BSG):c.1026C>T (p.Ile342=)	rs199862501	0.00038
NM_001728.4(BSG):c.366G>A (p.Ala122=)	rs148189655	0.00030
NM_001728.4(BSG):c.444C>T (p.Asp148=)	rs145196054

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