List of variants reported as benign for Deficiency of guanidinoacetate methyltransferase by ClinGen Cerebral Creatine Deficiency Syndromes Variant Curation Expert Panel, ClinGen

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000156.6(GAMT):c.626C>T (p.Thr209Met)	rs17851582	0.07010
NM_000156.6(GAMT):c.*11C>T	rs149268921	0.01866
NM_000156.6(GAMT):c.79T>C (p.Tyr27His)	rs200833152	0.00345
NM_000156.6(GAMT):c.392-7C>T	rs192416474	0.00144
NM_000156.6(GAMT):c.581T>C (p.Val194Ala)	rs147739199	0.00077
NM_000156.6(GAMT):c.279C>T (p.Asp93=)	rs144630886	0.00028
NM_000156.6(GAMT):c.182-265_182-228del	rs1404813118

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