List of variants in gene FGF23 reported as pathogenic for tumoral calcinosis, hyperphosphatemic, familial, 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_020638.3(FGF23):c.211A>G (p.Ser71Gly)	rs104894342	0.00001
GRCh37/hg19 12p13.32(chr12:4477393-4488878)
NM_020638.3(FGF23):c.287T>C (p.Met96Thr)	rs104894343
NM_020638.3(FGF23):c.386C>T (p.Ser129Phe)	rs104894344
NM_020638.3(FGF23):c.536G>A (p.Arg179Gln)	rs193922702

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