List of variants reported as likely pathogenic for Fabry disease by All of Us Research Program, National Institutes of Health

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000169.3(GLA):c.124A>C (p.Met42Leu)	rs797044613	0.00001
NM_000169.3(GLA):c.868A>C (p.Met290Leu)	rs375538532	0.00001
NM_000169.3(GLA):c.1165C>G (p.Pro389Ala)
NM_000169.3(GLA):c.560T>C (p.Met187Thr)	rs869312342
NM_000169.3(GLA):c.95T>C (p.Leu32Pro)	rs1569306168

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