List of variants reported as likely pathogenic for inherited thrombophilia by Mendelics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000133.4(F9):c.1346G>A (p.Arg449Gln)	rs143018900	0.00007
NM_000132.4(F8):c.1752+5G>T	rs2124094299

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