ClinVar Miner

List of variants reported as likely benign for Fabry disease by 3billion, Medical Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000169.3(GLA):c.196G>C (p.Glu66Gln)	rs104894833	0.00002
NM_000169.3(GLA):c.239G>C (p.Gly80Ala)	rs781838005	0.00001
NM_000169.3(GLA):c.61C>T (p.Leu21Phe)	rs782164084	0.00001

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