List of variants reported as uncertain significance for opsismodysplasia

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001567.4(INPPL1):c.1636G>A (p.Val546Ile)	rs376117918	0.00004
NM_001567.4(INPPL1):c.3244G>A (p.Gly1082Arg)	rs377723450	0.00004
NM_001567.4(INPPL1):c.349G>A (p.Val117Ile)	rs1354137878	0.00001
NM_001567.4(INPPL1):c.3563T>G (p.Leu1188Arg)	rs761199581	0.00001
NM_001567.4(INPPL1):c.1012G>T (p.Val338Leu)
NM_001567.4(INPPL1):c.1108_1155del (p.Ser370_Lys385del)	rs1565388201
NM_001567.4(INPPL1):c.1397T>A (p.Ile466Asn)
NM_001567.4(INPPL1):c.1497+5G>C
NM_001567.4(INPPL1):c.1963A>T (p.Ile655Phe)	rs752247882
NM_001567.4(INPPL1):c.2326+9C>T	rs370540380
NM_001567.4(INPPL1):c.2633G>A (p.Arg878His)
NM_001567.4(INPPL1):c.2839C>T (p.Pro947Ser)
NM_001567.4(INPPL1):c.3087C>G (p.His1029Gln)
NM_001567.4(INPPL1):c.3461C>G (p.Pro1154Arg)
NM_001567.4(INPPL1):c.724C>T (p.Pro242Ser)

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