List of variants in gene combination FANCA, ZNF276 reported as likely benign by PreventionGenetics, part of Exact Sciences

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.4249C>G (p.His1417Asp)	rs17227403	0.00362
NM_000135.4(FANCA):c.4303G>A (p.Ala1435Thr)	rs74977201	0.00176
NM_001113525.2(ZNF276):c.*841G>A	rs191404781	0.00092
NM_000135.4(FANCA):c.4332T>G (p.Pro1444=)	rs149531696	0.00072
NM_000135.4(FANCA):c.3792C>T (p.Ser1264=)	rs141128234	0.00030
NM_000135.4(FANCA):c.3801C>T (p.Gly1267=)	rs143772894	0.00022
NM_001113525.2(ZNF276):c.*1313A>G	rs368376237	0.00012
NM_000135.4(FANCA):c.3810G>A (p.Ser1270=)	rs138144828	0.00009
NM_000135.4(FANCA):c.3768A>G (p.Leu1256=)	rs747616573	0.00001
NM_000135.4(FANCA):c.3805C>T (p.Leu1269=)	rs757641646	0.00001
NM_000135.4(FANCA):c.3858C>T (p.His1286=)	rs761705192	0.00001
NM_000135.4(FANCA):c.3945G>C (p.Leu1315=)	rs941282193
NM_000135.4(FANCA):c.4350G>A (p.Gln1450=)	rs749315540
NM_001113525.2(ZNF276):c.*1223T>C	rs1383806921
NM_001113525.2(ZNF276):c.*485C>T

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