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

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		ClinVar version:

Total variants: 72

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HGVS	dbSNP	gnomAD frequency
NM_000169.3(GLA):c.619T>C (p.Tyr207His)	rs372416832	0.00005
NM_000169.3(GLA):c.1000-14T>C	rs397515868	0.00004
NM_000169.3(GLA):c.1184G>C (p.Gly395Ala)	rs375661583	0.00004
NM_000169.3(GLA):c.1261A>G (p.Met421Val)	rs144060196	0.00004
NM_000169.3(GLA):c.1175G>C (p.Arg392Thr)	rs782756052	0.00003
NM_000169.3(GLA):c.419A>C (p.Lys140Thr)	rs150228150	0.00003
NM_000169.3(GLA):c.1181T>C (p.Leu394Pro)	rs886044779	0.00002
NM_000169.3(GLA):c.481G>A (p.Asp161Asn)	rs1386622522	0.00002
NM_000169.3(GLA):c.579G>C (p.Arg193Ser)	rs782619655	0.00002
NM_000169.3(GLA):c.831G>C (p.Trp277Cys)	rs782196174	0.00002
NM_000169.3(GLA):c.1127T>A (p.Val376Glu)	rs1555984793	0.00001
NM_000169.3(GLA):c.1196G>C (p.Trp399Ser)	rs782449839	0.00001
NM_000169.3(GLA):c.247G>A (p.Asp83Asn)	rs782722577	0.00001
NM_000169.3(GLA):c.313A>G (p.Arg105Gly)	rs782092398	0.00001
NM_000169.3(GLA):c.361G>A (p.Ala121Thr)	rs782197638	0.00001
NM_000169.3(GLA):c.43G>A (p.Ala15Thr)	rs869312303	0.00001
NM_000169.3(GLA):c.596T>C (p.Val199Ala)	rs781871113	0.00001
NM_000169.3(GLA):c.734G>T (p.Trp245Leu)	rs398123220	0.00001
NM_000169.3(GLA):c.73G>A (p.Asp25Asn)	rs781788693	0.00001
NM_000169.3(GLA):c.-1A>C
NM_000169.3(GLA):c.1000-14dup
NM_000169.3(GLA):c.1000-9G>A	rs1928143594
NM_000169.3(GLA):c.1001G>A (p.Gly334Glu)
NM_000169.3(GLA):c.1007A>C (p.Asn336Thr)	rs1569302786
NM_000169.3(GLA):c.1048G>A (p.Ala350Thr)	rs1555984843
NM_000169.3(GLA):c.1101C>T (p.Ile367=)	rs1928129537
NM_000169.3(GLA):c.112A>G (p.Arg38Gly)	rs730880446
NM_000169.3(GLA):c.1164C>T (p.Leu388=)
NM_000169.3(GLA):c.119C>G (p.Pro40Arg)	rs398123199
NM_000169.3(GLA):c.178C>A (p.Pro60Thr)	rs727504689
NM_000169.3(GLA):c.19G>C (p.Glu7Gln)
NM_000169.3(GLA):c.209T>C (p.Met70Thr)
NM_000169.3(GLA):c.228G>A (p.Met76Ile)
NM_000169.3(GLA):c.239G>A (p.Gly80Asp)	rs781838005
NM_000169.3(GLA):c.260A>T (p.Glu87Val)
NM_000169.3(GLA):c.305C>T (p.Ser102Leu)
NM_000169.3(GLA):c.317T>C (p.Leu106Pro)
NM_000169.3(GLA):c.357G>T (p.Gln119His)
NM_000169.3(GLA):c.35G>T (p.Cys12Phe)
NM_000169.3(GLA):c.369+3G>A	rs1333591942
NM_000169.3(GLA):c.369+4A>T
NM_000169.3(GLA):c.377G>T (p.Ser126Ile)
NM_000169.3(GLA):c.388A>C (p.Lys130Gln)
NM_000169.3(GLA):c.44C>T (p.Ala15Val)
NM_000169.3(GLA):c.455A>T (p.Tyr152Phe)
NM_000169.3(GLA):c.493G>A (p.Asp165Asn)
NM_000169.3(GLA):c.548-3C>T
NM_000169.3(GLA):c.548-5T>A
NM_000169.3(GLA):c.557A>G (p.His186Arg)
NM_000169.3(GLA):c.56T>C (p.Leu19Pro)	rs1928592578
NM_000169.3(GLA):c.594T>G (p.Ile198Met)
NM_000169.3(GLA):c.595G>T (p.Val199Leu)
NM_000169.3(GLA):c.613C>G (p.Pro205Ala)
NM_000169.3(GLA):c.616C>T (p.Leu206Phe)	rs730880448
NM_000169.3(GLA):c.61C>G (p.Leu21Val)
NM_000169.3(GLA):c.64G>A (p.Val22Ile)
NM_000169.3(GLA):c.650C>T (p.Thr217Ile)
NM_000169.3(GLA):c.70T>A (p.Trp24Arg)	rs397515871
NM_000169.3(GLA):c.73G>T (p.Asp25Tyr)
NM_000169.3(GLA):c.74A>G (p.Asp25Gly)
NM_000169.3(GLA):c.752A>G (p.Glu251Gly)
NM_000169.3(GLA):c.781G>A (p.Gly261Ser)	rs886044878
NM_000169.3(GLA):c.790G>A (p.Asp264Asn)
NM_000169.3(GLA):c.802-14A>T
NM_000169.3(GLA):c.829T>G (p.Trp277Gly)	rs727504372
NM_000169.3(GLA):c.848A>G (p.Gln283Arg)
NM_000169.3(GLA):c.852G>A (p.Met284Ile)
NM_000169.3(GLA):c.871G>T (p.Ala291Ser)	rs869312439
NM_000169.3(GLA):c.913C>T (p.Pro305Ser)
NM_000169.3(GLA):c.946G>A (p.Val316Ile)	rs142217511
NM_000169.3(GLA):c.968C>G (p.Pro323Arg)	rs869312159
NM_000169.3(GLA):c.968C>T (p.Pro323Leu)

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