List of variants in gene GRM6 reported as likely pathogenic for perceptual disorders

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: 4

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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.118_132del (p.Thr40_Leu44del)	rs1237461749
NM_000843.4(GRM6):c.2497G>C (p.Gly833Arg)
NM_000843.4(GRM6):c.340C>T (p.Gln114Ter)

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