ClinVar Miner

List of variants in gene combination FAM20A, PRKAR1A reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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NM_017565.4(FAM20A):c.1511C>T (p.Thr504Ile) rs146689929
NM_212472.2(PRKAR1A):c.*1346A>G rs545417998
NM_212472.2(PRKAR1A):c.*138C>A rs28730842
NM_212472.2(PRKAR1A):c.*151A>G rs11540571
NM_212472.2(PRKAR1A):c.*156C>T rs535007635
NM_212472.2(PRKAR1A):c.*1606A>G rs144632545
NM_212472.2(PRKAR1A):c.*172_*175del rs201146882
NM_212472.2(PRKAR1A):c.*1835del rs138320066
NM_212472.2(PRKAR1A):c.*1837G>T rs201999343
NM_212472.2(PRKAR1A):c.*2018C>T rs540185706
NM_212472.2(PRKAR1A):c.*2197G>A rs533508012
NM_212472.2(PRKAR1A):c.*672T>C rs546125048
NM_212472.2(PRKAR1A):c.*722A>G rs555951287
NM_212472.2(PRKAR1A):c.*759C>T rs62087489
NM_212472.2(PRKAR1A):c.*795G>T rs150031305
NM_212472.2(PRKAR1A):c.*812A>C rs116996069
NM_212472.2(PRKAR1A):c.*847A>G rs144299673
NM_212472.2(PRKAR1A):c.*893G>C rs186568426
NM_212472.2(PRKAR1A):c.1143C>G (p.Val381=) rs755043531

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