Variants in gene GRM1 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001278064.2(GRM1):c.2725A>C (p.Met909Leu)	rs138759146	0.00020
NM_001278064.2(GRM1):c.2026G>A (p.Val676Met)	rs752403373	0.00003
NM_001278064.2(GRM1):c.3300C>A (p.Ser1100Arg)	rs1227591846	0.00001
NM_001278064.2(GRM1):c.2796C>G (p.Pro932=)	rs1583494731
NM_001278064.2(GRM1):c.3138G>A (p.Pro1046=)
NM_001278064.2(GRM1):c.885A>C (p.Thr295=)

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