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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000843.4(GRM6):c.712C>T (p.Arg238Ter)	rs199663175	0.00018
NM_000843.4(GRM6):c.3G>T (p.Met1Ile)	rs942517034	0.00004
NM_000843.4(GRM6):c.208G>T (p.Glu70Ter)	rs1353889281	0.00001
NC_000005.10:g.178991560del	rs281865186
NC_000005.9:g.(?_178409993)_(178416072_?)del
NM_000843.4(GRM6):c.152_174dup (p.Gln59fs)	rs1760743459
NM_000843.4(GRM6):c.165_177del (p.Arg55_Ala56insTer)	rs751696722
NM_000843.4(GRM6):c.208del (p.Glu70fs)
NM_000843.4(GRM6):c.222C>A (p.Tyr74Ter)	rs778393434
NM_000843.4(GRM6):c.222C>G (p.Tyr74Ter)	rs778393434
NM_000843.4(GRM6):c.577del (p.Val193fs)	rs781463257
NM_000843.4(GRM6):c.597C>A (p.Tyr199Ter)
NM_000843.4(GRM6):c.716_717del (p.Glu239fs)
NM_000843.4(GRM6):c.727dup	rs281865186
NM_000843.4(GRM6):c.768_789dup (p.Ile264fs)
NM_000843.4(GRM6):c.824dup (p.Ile276fs)
NM_000843.4(GRM6):c.86_87del (p.Ala29fs)

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