ClinVar Miner

List of variants in gene CDC73 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_024529.4(CDC73):c.*1083A>T rs367704451
NM_024529.4(CDC73):c.*1267A>G rs78218016
NM_024529.4(CDC73):c.*1499T>A rs138503809
NM_024529.4(CDC73):c.*1833A>G rs150894778
NM_024529.4(CDC73):c.*2085G>C rs150030810
NM_024529.4(CDC73):c.*2304T>G rs144363422
NM_024529.4(CDC73):c.*2427T>C rs372585994
NM_024529.4(CDC73):c.*2677G>A rs192018514
NM_024529.4(CDC73):c.*2950A>G rs144681513
NM_024529.4(CDC73):c.*3507G>T rs151216299
NM_024529.4(CDC73):c.*3524A>G rs548190260
NM_024529.4(CDC73):c.*3786T>A rs74130943
NM_024529.4(CDC73):c.*3786T>C rs74130943
NM_024529.4(CDC73):c.*518A>G rs190433473
NM_024529.4(CDC73):c.*580A>T rs191600804
NM_024529.4(CDC73):c.-10G>T rs188082584
NM_024529.4(CDC73):c.-11G>A rs80356643
NM_024529.4(CDC73):c.-95G>A rs143969598
NM_024529.4(CDC73):c.1032T>G (p.Val344=) rs148612206
NM_024529.4(CDC73):c.1185A>G (p.Gln395=) rs116358657
NM_024529.4(CDC73):c.534A>G (p.Ser178=) rs150365980
NM_024529.5(CDC73):c.*3063G>A

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