List of variants in gene FGF23 reported as likely benign for familial tumoral calcinosis

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_020638.3(FGF23):c.*388G>A	rs13312795	0.00731
NM_020638.3(FGF23):c.583C>T (p.Pro195Ser)	rs13312793	0.00310
NM_020638.3(FGF23):c.423G>T (p.Ala141=)	rs13312792	0.00290
NM_020638.3(FGF23):c.*29C>G	rs71534281	0.00140
NM_020638.3(FGF23):c.342G>A (p.Arg114=)	rs138972495	0.00048
NM_020638.3(FGF23):c.*2062A>C	rs558079364	0.00028
NM_020638.3(FGF23):c.*998C>G	rs71583766	0.00017
NM_020638.3(FGF23):c.51C>T (p.Cys17=)	rs752187740	0.00001
NM_020638.3(FGF23):c.-53C>G	rs187035769
NM_020638.3(FGF23):c.315+15del	rs771309899
NM_020638.3(FGF23):c.555G>A (p.Ser185=)	rs115283398
NM_020638.3(FGF23):c.555G>C (p.Ser185=)	rs115283398

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