List of variants in gene F8 reported as uncertain significance for Thrombophilia, X-linked, due to factor 8 defect

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

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.3836G>A (p.Arg1279Lys)	rs139451429	0.00017
NM_000132.4(F8):c.1337G>A (p.Arg446Gln)	rs781889613	0.00010
NM_000132.4(F8):c.3701A>T (p.His1234Leu)	rs145507297	0.00006
NM_000132.4(F8):c.4531G>A (p.Val1511Ile)	rs186353717	0.00006
NM_000132.4(F8):c.3986G>A (p.Arg1329His)	rs782767347	0.00001

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