List of variants studied for Fanconi anemia complementation group O by Illumina Laboratory Services, Illumina

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.90G>A (p.Ala30=)	rs115414895	0.01193
NM_058216.3(RAD51C):c.186A>G (p.Gln62=)	rs28363303	0.00322
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	rs147241704	0.00207
NM_058216.3(RAD51C):c.146-8A>G	rs201079501	0.00074
NM_058216.3(RAD51C):c.145+12T>G	rs377297129	0.00024
NM_058216.3(RAD51C):c.721G>A (p.Val241Met)	rs184033132	0.00004
NM_058216.3(RAD51C):c.1102C>T (p.Arg368Trp)	rs587780253	0.00003
NM_058216.3(RAD51C):c.404+7T>C	rs1350153132	0.00001
NM_058216.3(RAD51C):c.435A>G (p.Pro145=)	rs555235745	0.00001
NM_058216.3(RAD51C):c.601C>G (p.Leu201Val)	rs531838785	0.00001
NM_058216.3(RAD51C):c.404+13G>A	rs547506164
NM_058216.3(RAD51C):c.822T>G (p.Asn274Lys)	rs2048501654
NM_058216.3(RAD51C):c.87T>C (p.Ser29=)	rs786203249

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