List of variants reported as uncertain significance for Tumoral calcinosis, hyperphosphatemic, familial, 3 by Fulgent Genetics, Fulgent Genetics

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Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_004795.4(KL):c.1764G>T (p.Met588Ile)	rs543489938	0.00014
NM_004795.4(KL):c.1882C>T (p.Arg628Cys)	rs200940225	0.00012
NM_004795.4(KL):c.1858C>T (p.Arg620Cys)	rs34292549	0.00011
NM_004795.4(KL):c.2862G>A (p.Pro954=)	rs387907447	0.00009
NM_004795.4(KL):c.2069C>T (p.Pro690Leu)	rs146275953	0.00007
NM_004795.4(KL):c.2251A>G (p.Arg751Gly)	rs373177691	0.00007
NM_004795.4(KL):c.2557C>T (p.Arg853Cys)	rs147992424	0.00006
NM_004795.4(KL):c.2057C>T (p.Thr686Met)	rs141695559	0.00004
NM_004795.4(KL):c.2513G>C (p.Trp838Ser)	rs199812311	0.00004
NM_004795.4(KL):c.398T>A (p.Phe133Tyr)	rs749356037	0.00004
NM_004795.4(KL):c.560C>T (p.Pro187Leu)	rs761695698	0.00004
NM_004795.4(KL):c.1780C>T (p.Arg594Cys)	rs138511256	0.00002
NM_004795.4(KL):c.497A>G (p.Asn166Ser)	rs387907444	0.00002
NM_004795.4(KL):c.944A>G (p.Glu315Gly)	rs759972130	0.00002
NM_004795.4(KL):c.1331-3C>A	rs748430461	0.00001
NM_004795.4(KL):c.1811C>A (p.Pro604His)	rs751229348	0.00001
NM_004795.4(KL):c.254A>G (p.Lys85Arg)	rs1190809246	0.00001
NM_004795.4(KL):c.257G>A (p.Gly86Asp)	rs1477759912	0.00001
NM_004795.4(KL):c.2684T>C (p.Ile895Thr)	rs387907441	0.00001
NM_004795.4(KL):c.535C>T (p.Arg179Trp)	rs746435085	0.00001
NM_004795.4(KL):c.1462TTG[1] (p.Leu489del)	rs777919048
NM_004795.4(KL):c.2296G>C (p.Gly766Arg)	rs114752661
NM_004795.4(KL):c.4C>T (p.Pro2Ser)	rs1425467064
NM_004795.4(KL):c.721dup (p.Tyr241fs)	rs2138184030

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