ClinVar Miner

List of variants reported as benign for hemophilia A by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_000132.4(F8):c.1010-27G>A rs7058826 0.13707
NM_000132.4(F8):c.*29C>T rs5986887 0.01323
NM_000132.4(F8):c.1444-22T>C rs5986899 0.01075
NM_000132.4(F8):c.670+31C>G rs34277626 0.00585
NM_000132.4(F8):c.601+17G>A rs200951849 0.00024
NM_000132.4(F8):c.1866T>C (p.Leu622=) rs1800290 0.00021
NM_000132.4(F8):c.6849C>T (p.Ser2283=) rs1319284046 0.00001
NM_000132.4(F8):c.5493C>G (p.Thr1831=) rs1603432997

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