List of variants in gene F11 reported as likely 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)
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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.1717-48A>G	rs5966	0.06916
NM_000128.4(F11):c.-54G>A	rs4253814	0.01170
NM_000128.4(F11):c.1016G>T (p.Cys339Phe)	rs5967	0.00586
NM_000128.4(F11):c.1304+12G>A	rs116667976	0.00295
NM_000128.4(F11):c.453C>T (p.Tyr151=)	rs34807019	0.00248
NM_000128.4(F11):c.*884C>T	rs117035365	0.00024
NM_000128.4(F11):c.1843G>A (p.Val615Met)	rs202061241	0.00016
NM_000128.4(F11):c.1683C>T (p.Ala561=)	rs770473069	0.00003
NM_000128.4(F11):c.1304+25_1304+28del	rs778294619
NM_000128.4(F11):c.1481-34G>T	rs2289253
NM_000128.4(F11):c.1576+51C>A	rs2289254

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