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: 3

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HGVS	dbSNP	gnomAD frequency
NM_198904.4(GABRG2):c.798T>C (p.Phe266=)	rs115126975	0.00063
NM_198904.4(GABRG2):c.107+12C>T	rs369466385	0.00024
NM_198904.4(GABRG2):c.632-1212C>T	rs587780948	0.00004

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