List of variants in gene combination FANCI, POLG reported as uncertain significance for Fanconi anemia complementation group I

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.3644-184T>C	rs115758754	0.00173
NM_002693.3(POLG):c.*63A>G	rs552236933	0.00061
NM_002693.3(POLG):c.*100G>A	rs770839560	0.00012
NM_002693.3(POLG):c.3644-16T>C	rs536522307	0.00012
NM_002693.3(POLG):c.*122G>A	rs886051517	0.00009
NM_002693.3(POLG):c.*44G>C	rs563185483	0.00009
NM_001113378.2(FANCI):c.3946G>A (p.Gly1316Arg)	rs369058619	0.00007
NM_002693.3(POLG):c.3650C>T (p.Ala1217Val)	rs199751339	0.00006
NM_002693.3(POLG):c.3701G>A (p.Arg1234Gln)	rs750792237	0.00006
NM_002693.3(POLG):c.3644-116T>C	rs777372106	0.00003
NM_001113378.2(FANCI):c.3931G>T (p.Ala1311Ser)	rs754573704	0.00001
NM_001113378.2(FANCI):c.*614T>G	rs886051521
NM_001113378.2(FANCI):c.*662C>G	rs560246181
NM_001113378.2(FANCI):c.3985T>A (p.Ter1329Lys)	rs1411317487
NM_002693.3(POLG):c.*49G>A	rs758880377
NM_002693.3(POLG):c.3700C>G (p.Arg1234Gly)	rs144346886

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