Variants in gene GLRA1 with conflicting interpretations "pathogenic" and "pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000171.4(GLRA1):c.690C>A (p.Tyr230Ter)	rs121918415
NM_000171.4(GLRA1):c.777C>G (p.Ser259Arg)	rs121918417
NM_000171.4(GLRA1):c.815T>A (p.Ile272Asn)	rs121918409
NM_000171.4(GLRA1):c.832C>A (p.Pro278Thr)	rs121918413
NM_000171.4(GLRA1):c.862G>A (p.Val288Met)	rs121918416
NM_000171.4(GLRA1):c.882G>C (p.Gln294His)	rs121918411
NM_000171.4(GLRA1):c.896G>A (p.Arg299Gln)	rs121918408
NM_000171.4(GLRA1):c.896G>T (p.Arg299Leu)	rs121918408
NM_000171.4(GLRA1):c.910A>G (p.Lys304Glu)	rs121918412
NM_000171.4(GLRA1):c.920A>G (p.Tyr307Cys)	rs121918410
NM_001146040.1(GLRA1):c.(?_-287)_(912+?)del

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