Variants in gene GABRG2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP
NM_198903.2(GABRG2):c.751+4C>T	rs587780948
NM_198903.2(GABRG2):c.918T>C (p.Phe306=)	rs115126975

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