List of variants reported as uncertain significance for Fanconi anemia complementation group O by Counsyl

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.146-8A>G	rs201079501	0.00074
NM_058216.3(RAD51C):c.890T>C (p.Leu297Pro)	rs143026267	0.00017
NM_058216.3(RAD51C):c.784T>G (p.Leu262Val)	rs149331537	0.00014
NM_058216.3(RAD51C):c.431T>C (p.Ile144Thr)	rs28363307	0.00010
NM_058216.3(RAD51C):c.506T>C (p.Val169Ala)	rs587780256	0.00009
NM_058216.3(RAD51C):c.134A>G (p.Glu45Gly)	rs587781383	0.00006
NM_058216.3(RAD51C):c.14C>T (p.Thr5Met)	rs201523760	0.00006
NM_058216.3(RAD51C):c.492T>G (p.Phe164Leu)	rs573992101	0.00006
NM_058216.3(RAD51C):c.635G>A (p.Arg212His)	rs200857129	0.00004
NM_058216.3(RAD51C):c.77A>T (p.Lys26Met)	rs746026526	0.00003
NM_058216.3(RAD51C):c.719T>C (p.Ile240Thr)	rs539341386	0.00002
NM_058216.3(RAD51C):c.379C>A (p.Pro127Thr)	rs587782222	0.00001
NM_058216.3(RAD51C):c.115C>G (p.Leu39Val)	rs759149207
NM_058216.3(RAD51C):c.724G>A (p.Asp242Asn)	rs876659188
NM_058216.3(RAD51C):c.862A>G (p.Thr288Ala)	rs587781574

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