List of variants in gene GAMT reported as benign for brain disorder

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000156.6(GAMT):c.460-31G>A	rs55776826	0.14411
NM_000156.6(GAMT):c.*11C>T	rs149268921	0.01866
NM_000156.6(GAMT):c.570+165G>A	rs74253480	0.00981
NM_000156.6(GAMT):c.392-7C>T	rs192416474	0.00144
NM_000156.6(GAMT):c.348G>A (p.Leu116=)	rs117884619	0.00133
NM_000156.6(GAMT):c.581T>C (p.Val194Ala)	rs147739199	0.00077
NM_000156.6(GAMT):c.182-18C>T	rs376709081	0.00033
NM_000156.6(GAMT):c.279C>T (p.Asp93=)	rs144630886	0.00028
NM_000156.6(GAMT):c.182-265_182-228del	rs1404813118
NM_000156.6(GAMT):c.328-13del
NM_000156.6(GAMT):c.391+47A>G	rs73515058

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