List of variants studied for Hereditary factor XI deficiency disease by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.325G>A (p.Ala109Thr)	rs768474112	0.00002
NM_000128.4(F11):c.1432G>A (p.Gly478Arg)	rs542967227	0.00001
NM_000128.4(F11):c.1135+4A>C
NM_000128.4(F11):c.1234C>T (p.Gln412Ter)	rs538083600
NM_000128.4(F11):c.1335C>G (p.Tyr445Ter)
NM_000128.4(F11):c.508A>T (p.Thr170Ser)

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