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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_198904.4(GABRG2):c.530G>A (p.Arg177Gln)	rs1445637165	0.00001
NM_198904.4(GABRG2):c.247C>A (p.Pro83Thr)
NM_198904.4(GABRG2):c.373C>T (p.Arg125Cys)	rs2113325423
NM_198904.4(GABRG2):c.893A>C (p.Lys298Thr)	rs1764627724
NM_198904.4(GABRG2):c.941C>A (p.Thr314Lys)

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