List of variants reported as likely benign for Fabry disease by Genome-Nilou Lab

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000169.3(GLA):c.8T>C (p.Leu3Pro)	rs150547672	0.00098
NM_000169.3(GLA):c.376A>G (p.Ser126Gly)	rs149391489	0.00043
NM_000169.3(GLA):c.123C>T (p.Thr41=)	rs137902198	0.00017
NM_000169.3(GLA):c.-8C>G	rs371291716	0.00014
NM_000169.3(GLA):c.48T>G (p.Leu16=)	rs201449986	0.00011
NM_000169.3(GLA):c.865A>G (p.Ile289Val)	rs140329381	0.00009
NM_000169.3(GLA):c.945C>T (p.Asp315=)	rs151208856	0.00009
NM_000169.3(GLA):c.1261A>G (p.Met421Val)	rs144060196	0.00004
NM_000169.3(GLA):c.639+6A>C	rs200096940	0.00003
NM_000169.3(GLA):c.714T>C (p.Ser238=)	rs397515872	0.00003
NM_000169.3(GLA):c.196G>C (p.Glu66Gln)	rs104894833	0.00002
NM_000169.3(GLA):c.26A>G (p.His9Arg)	rs1555987214	0.00001
NM_000169.3(GLA):c.1102G>A (p.Ala368Thr)	rs144994244
NM_000169.3(GLA):c.1102G>C (p.Ala368Pro)	rs144994244
NM_000169.3(GLA):c.525C>G (p.Asp175Glu)	rs782722844

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