ClinVar Miner

List of variants reported as uncertain significance for hemophilia A by ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology

Included ClinVar conditions (4):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.1601T>C (p.Val534Ala)	rs1557281261
NM_000132.4(F8):c.1835G>T (p.Arg612Leu)	rs782473762
NM_000132.4(F8):c.2T>A (p.Met1Lys)

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