List of variants reported as likely benign for brachydactyly type B1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_004560.4(ROR2):c.717C>T (p.Cys239=)	rs56302651	0.00597
NM_004560.4(ROR2):c.937+10C>T	rs201083970	0.00310
NM_004560.4(ROR2):c.7C>T (p.Arg3Trp)	rs539329891	0.00261
NM_004560.4(ROR2):c.175+17A>G	rs372392835	0.00243
NM_004560.4(ROR2):c.372C>T (p.Asp124=)	rs145568368	0.00241
NM_004560.4(ROR2):c.494+17C>T	rs201549038	0.00053
NM_004560.4(ROR2):c.721G>A (p.Ala241Thr)	rs141577636	0.00032
NM_004560.4(ROR2):c.1572G>A (p.Glu524=)	rs138666116	0.00024
NM_004560.4(ROR2):c.2274G>A (p.Ser758=)	rs139915017	0.00016
NM_004560.4(ROR2):c.525G>A (p.Gln175=)	rs147616624	0.00016
NM_004560.4(ROR2):c.2613A>C (p.Thr871=)	rs751280391	0.00015
NM_004560.4(ROR2):c.1524G>A (p.Thr508=)	rs114395148	0.00013
NM_004560.4(ROR2):c.2586C>T (p.His862=)	rs56158629	0.00011
NM_004560.4(ROR2):c.97+7T>C	rs377341845	0.00010
NM_004560.4(ROR2):c.2604C>T (p.Ser868=)	rs369150056	0.00007
NM_004560.4(ROR2):c.485A>G (p.His162Arg)	rs569718323	0.00007
NM_004560.4(ROR2):c.1863G>A (p.Val621=)	rs778321761	0.00006
NM_004560.4(ROR2):c.1712A>G (p.His571Arg)	rs376970201	0.00005
NM_004560.4(ROR2):c.1998C>T (p.Tyr666=)	rs773389306	0.00004
NM_004560.4(ROR2):c.2724C>T (p.Thr908=)	rs374824850	0.00004
NM_004560.4(ROR2):c.888C>T (p.Asp296=)	rs755825636	0.00004
NM_004560.4(ROR2):c.2451C>T (p.Leu817=)	rs200396791	0.00003
NM_004560.4(ROR2):c.2478G>A (p.Pro826=)	rs145213893	0.00002
NM_004560.4(ROR2):c.954C>T (p.Asn318=)	rs553026289	0.00002
NM_004560.4(ROR2):c.1605C>T (p.Asn535=)	rs769352677	0.00001
NM_004560.4(ROR2):c.1104C>T (p.Pro368=)	rs200675570
NM_004560.4(ROR2):c.2442G>A (p.Pro814=)	rs185808139

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