List of variants in gene CDC73 reported as pathogenic for Hyperparathyroidism 1

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_024529.5(CDC73):c.131+1G>A	rs587776558
NM_024529.5(CDC73):c.191T>C (p.Leu64Pro)	rs121434264
NM_024529.5(CDC73):c.271C>T (p.Arg91Ter)	rs1558280170
NM_024529.5(CDC73):c.520_523del (p.Ser174fs)
NM_024529.5(CDC73):c.626_629del (p.Lys209fs)	rs2103126261
NM_024529.5(CDC73):c.679_680insAG (p.Arg227fs)	rs80356649
NM_024529.5(CDC73):c.685A>T (p.Arg229Ter)

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