List of variants in gene F12 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)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000505.4(F12):c.398-12C>T	rs56285942	0.00495
NC_000005.10:g.177409584C>G	rs41309132	0.00297
NM_000505.4(F12):c.418C>G (p.Leu140Val)	rs35515200	0.00247
NM_000505.4(F12):c.-62C>T	rs187018744	0.00223
NM_000505.4(F12):c.1027G>C (p.Ala343Pro)	rs183643295	0.00115
NM_000505.4(F12):c.-8C>T	rs369991760	0.00032

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