List of variants in gene FGF23 reported as benign for calcium metabolic disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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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
NM_020638.3(FGF23):c.211+19T>C	rs141828684	0.00162
NM_020638.3(FGF23):c.555G>C (p.Ser185=)	rs115283398

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