List of variants in gene F13A1 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)
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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000129.4(F13A1):c.1747+27C>G	rs380058	0.98624
NM_000129.4(F13A1):c.-19+12A>C	rs2815822	0.88252
NM_000129.4(F13A1):c.*126T>C	rs1050782	0.52358
NM_000129.4(F13A1):c.1217-23C>T	rs5978	0.26684
NM_000129.4(F13A1):c.103G>T (p.Val35Leu)	rs5985	0.22002
NM_000129.4(F13A1):c.1954G>C (p.Glu652Gln)	rs5988	0.21467
NM_000129.4(F13A1):c.1909-29G>C	rs2274394	0.21456
NM_000129.4(F13A1):c.1694C>T (p.Pro565Leu)	rs5982	0.18893
NM_000129.4(F13A1):c.*160G>A	rs1050783	0.18575
NM_000129.4(F13A1):c.996A>C (p.Pro332=)	rs5981	0.15230
NM_000129.4(F13A1):c.*995G>T	rs3024466	0.13914
NM_000129.4(F13A1):c.1217-24C>T	rs5977	0.12083
NM_000129.4(F13A1):c.1704A>G (p.Glu568=)	rs5986	0.07753
NM_000129.4(F13A1):c.1951G>A (p.Val651Ile)	rs5987	0.05207
NM_000129.4(F13A1):c.*89A>G	rs3024462	0.04627
NM_000129.4(F13A1):c.*743G>A	rs12862	0.04625
NM_000129.4(F13A1):c.*221G>A	rs3024464	0.04624

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