Variants in gene GABRA1 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001127644.2(GABRA1):c.1020A>C (p.Arg340Ser)	rs1561587910
NM_001127644.2(GABRA1):c.610C>T (p.Arg204Cys)
NM_001127644.2(GABRA1):c.640C>T (p.Arg214Cys)	rs727503940
NM_001127644.2(GABRA1):c.799C>A (p.Leu267Ile)	rs796052492
NM_001127644.2(GABRA1):c.851T>C (p.Val284Ala)	rs794727962
NM_001127644.2(GABRA1):c.859G>A (p.Val287Ile)	rs796052493
NM_001127644.2(GABRA1):c.884C>T (p.Thr295Ile)	rs796052496
NM_001127644.2(GABRA1):c.923C>A (p.Ala308Asp)	rs1554087620
NM_001127644.2(GABRA1):c.932C>T (p.Thr311Ile)	rs1581220210

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