List of variants in gene GRM6 reported as likely pathogenic for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000843.4(GRM6):c.137C>T (p.Pro46Leu)	rs62638197	0.00009
NM_000843.4(GRM6):c.448G>A (p.Gly150Ser)	rs62638202	0.00003
NM_000843.4(GRM6):c.722-2del	rs758498215	0.00001
NM_000843.4(GRM6):c.721+1G>C
NM_000843.4(GRM6):c.722-2A>C

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