List of variants reported as likely benign for Hyperparathyroidism 1 by Illumina Laboratory Services, Illumina

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_024529.5(CDC73):c.*1267A>G	rs78218016	0.01764
NM_024529.5(CDC73):c.*580A>T	rs191600804	0.01264
NM_024529.5(CDC73):c.1185A>G (p.Gln395=)	rs116358657	0.00511
NM_024529.5(CDC73):c.*2304T>G	rs144363422	0.00424
NM_024529.5(CDC73):c.*2085G>C	rs150030810	0.00217
NM_024529.5(CDC73):c.*12C>A	rs193025205	0.00196
NM_024529.5(CDC73):c.*518A>G	rs190433473	0.00195
NM_024529.5(CDC73):c.-95G>A	rs143969598	0.00133
NM_024529.5(CDC73):c.33C>T (p.Tyr11=)	rs150951102	0.00094
NM_024529.5(CDC73):c.*3524A>G	rs548190260	0.00071
NM_024529.5(CDC73):c.1032T>G (p.Val344=)	rs148612206	0.00070
NM_024529.5(CDC73):c.-10G>T	rs188082584	0.00024
NM_024529.5(CDC73):c.*2427T>C	rs372585994	0.00013
NM_024529.5(CDC73):c.840G>A (p.Leu280=)	rs10921320	0.00012
NM_024529.5(CDC73):c.*2677G>A	rs192018514	0.00010
NM_024529.5(CDC73):c.*1083A>T	rs367704451	0.00006
NM_024529.5(CDC73):c.*3063G>A	rs182545034	0.00001
NM_024529.5(CDC73):c.*3786T>C	rs74130943

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