List of variants reported as likely benign for congenital factor X deficiency by Illumina Laboratory Services, Illumina

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_019616.4(F7):c.*1146A>G	rs3093255	0.04222
NM_019616.4(F7):c.*673A>G	rs3093251	0.03895
NM_000504.4(F10):c.-40C>T	rs3212994	0.03388
NM_019616.4(F7):c.*1275A>G	rs3093257	0.03241
NM_019616.4(F7):c.*639G>A	rs3093250	0.02923
NM_019616.4(F7):c.*888G>A	rs79733913	0.02191
NM_000504.4(F10):c.399C>T (p.Asn133=)	rs5962	0.01840
NM_019616.4(F7):c.*1649G>A	rs3093259	0.01345
NM_019616.4(F7):c.*533A>C	rs116688254	0.00744
NM_000504.4(F10):c.396C>T (p.Asp132=)	rs111737184	0.00287
NM_000504.4(F10):c.71-8C>T	rs374210821	0.00010
NM_019616.4(F7):c.*1240C>G	rs3093256
NM_019616.4(F7):c.*82T>C	rs368359845

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