List of variants in gene SERPINF1 reported as benign for bone 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_002615.7(SERPINF1):c.963T>C (p.Tyr321=)	rs6828	0.76939
NM_002615.7(SERPINF1):c.440-39C>T	rs4274474	0.75763
NM_002615.7(SERPINF1):c.215C>T (p.Thr72Met)	rs1136287	0.69033
NM_002615.7(SERPINF1):c.390T>C (p.Thr130=)	rs8074840	0.27779
NM_002615.7(SERPINF1):c.440-28C>T	rs4274475	0.27322
NM_002615.7(SERPINF1):c.644-14A>T	rs3891224	0.12986
NM_002615.7(SERPINF1):c.643+9G>A	rs12103559	0.07824
NM_002615.6(SERPINF1):c.-86C>A	rs9913583	0.06510
NM_002615.7(SERPINF1):c.395C>G (p.Pro132Arg)	rs1804145	0.02056
NM_002615.7(SERPINF1):c.509C>T (p.Thr170Met)	rs762383656	0.00002
NM_002615.7(SERPINF1):c.502G>T (p.Val168Phe)	rs1597352279
NM_002615.7(SERPINF1):c.85-14C>A	rs200755661

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