List of variants in gene F10 reported as benign for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000504.4(F10):c.865+33A>G	rs2031184	0.93642
NM_000504.4(F10):c.232-17T>C	rs2251102	0.79208
NM_000504.4(F10):c.792C>T (p.Thr264=)	rs5960	0.72493
NM_000504.4(F10):c.574G>A (p.Gly192Arg)	rs3211783	0.02730
NM_000504.4(F10):c.90G>C (p.Gln30His)	rs5961	0.01285
NM_000504.4(F10):c.111G>A (p.Arg37=)	rs115112448	0.00649
NM_000504.4(F10):c.1115G>C (p.Arg372Pro)	rs142699098

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