List of variants reported as likely benign for dysostosis by Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_020436.5(SALL4):c.2041G>A (p.Ala681Thr)	rs147385529	0.00056
NM_207037.2(TCF12):c.*3A>G	rs1224019481	0.00001

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