Variants in gene GABRG2 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_198904.4(GABRG2):c.1217_1218del (p.Gln406fs)	rs1554101202
NM_198904.4(GABRG2):c.1297C>T (p.Arg433Ter)	rs1554101224
NM_198904.4(GABRG2):c.316G>A (p.Ala106Thr)	rs796052505
NM_198904.4(GABRG2):c.471del (p.Ala158fs)	rs1554097890
NM_198904.4(GABRG2):c.501C>A (p.Asn167Lys)	rs1581351046
NM_198904.4(GABRG2):c.670C>T (p.Arg224Ter)	rs1045493304
NM_198904.4(GABRG2):c.974C>T (p.Ser325Leu)	rs1581453572
NM_198904.4(GABRG2):c.992A>G (p.Tyr331Cys)	rs1390117240

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