List of variants reported as likely pathogenic for bone disorder by Clinical Genetics Laboratory, Skane University Hospital Lund

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000088.4(COL1A1):c.1399G>A (p.Gly467Arg)	rs2144573313
NM_000451.4(SHOX):c.458G>T (p.Arg153Leu)	rs137852555
NM_002335.4(LRP5):c.590C>G (p.Pro197Arg)

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