List of variants reported as benign for tumoral calcinosis, hyperphosphatemic, familial, 2 by Illumina Laboratory Services, Illumina

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_020638.3(FGF23):c.*1429A>T	rs11063112	0.22976
NM_020638.3(FGF23):c.716C>T (p.Thr239Met)	rs7955866	0.11385
NM_020638.3(FGF23):c.*1079A>G	rs13312798	0.01230
NM_020638.3(FGF23):c.*23T>G	rs13312794	0.00893
NM_020638.3(FGF23):c.*1971T>C	rs140798293	0.00403
NM_020638.3(FGF23):c.*1471C>A	rs114125104	0.00388
NM_020638.3(FGF23):c.*1219C>T	rs115582772	0.00387
NM_020638.3(FGF23):c.*1316C>A	rs138576496	0.00387
NM_020638.3(FGF23):c.*1464T>C	rs144700678	0.00387
NM_020638.3(FGF23):c.423G>T (p.Ala141=)	rs13312792	0.00290
NM_020638.3(FGF23):c.*553C>A	rs80210924	0.00163

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