List of variants reported as pathogenic for thrombophilia, X-linked, due to factor 9 defect by Mendelics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000133.4(F9):c.1345C>T (p.Arg449Trp)	rs757996262	0.00009
NM_000133.4(F9):c.316G>A (p.Gly106Ser)	rs137852233	0.00004
NM_000133.4(F9):c.572G>A (p.Arg191His)	rs137852238	0.00001
NM_000133.4(F9):c.890T>A (p.Ile297Asn)	rs752084251	0.00001

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