List of variants reported as benign for osteogenesis imperfecta type 6

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_002615.7(SERPINF1):c.963T>C (p.Tyr321=)	rs6828	0.77455
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	0.27102
NM_002615.7(SERPINF1):c.440-28C>T	rs4274475	0.26633
NM_002615.7(SERPINF1):c.644-14A>T	rs3891224	0.12986
NM_002615.7(SERPINF1):c.643+9G>A	rs12103559	0.07824
NM_002615.7(SERPINF1):c.395C>G (p.Pro132Arg)	rs1804145	0.02133
NM_002615.7(SERPINF1):c.151G>A (p.Val51Met)	rs150899084	0.00047
NM_002615.7(SERPINF1):c.509C>T (p.Thr170Met)	rs762383656	0.00002
NM_002615.7(SERPINF1):c.167C>G (p.Ala56Gly)	rs76119062
NM_002615.7(SERPINF1):c.502G>T (p.Val168Phe)	rs1597352279
NM_002615.7(SERPINF1):c.85-14C>A	rs200755661

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