List of variants in gene combination FANCA, ZNF276 reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_001113525.2(ZNF276):c.*1316C>T	rs9282680	0.01028
NM_001113525.2(ZNF276):c.*768dup	rs55873203	0.00841
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_000135.4(FANCA):c.4036G>A (p.Ala1346Thr)	rs17227396	0.00056
NM_001113525.2(ZNF276):c.*470A>C	rs372268907	0.00049
NM_000135.4(FANCA):c.3981C>T (p.His1327=)	rs141278771	0.00036
NM_000135.4(FANCA):c.3801C>T (p.Gly1267=)	rs143772894	0.00022
NM_000135.4(FANCA):c.4302C>T (p.Ala1434=)	rs142784426	0.00021
NM_000135.4(FANCA):c.3912A>G (p.Ala1304=)	rs545021222	0.00019
NM_001113525.2(ZNF276):c.*1313A>G	rs368376237	0.00012
NM_001113525.2(ZNF276):c.*471G>C	rs368506826	0.00012
NM_000135.4(FANCA):c.3810G>A (p.Ser1270=)	rs138144828	0.00009
NM_000135.4(FANCA):c.4226G>A (p.Arg1409Gln)	rs370507983	0.00006
NM_000135.4(FANCA):c.4284C>T (p.Cys1428=)	rs367630825	0.00004
NM_000135.4(FANCA):c.4038G>A (p.Ala1346=)	rs755479861	0.00003
NM_000135.4(FANCA):c.4108G>T (p.Ala1370Ser)	rs750839091	0.00003
NM_000135.4(FANCA):c.3876C>T (p.Leu1292=)	rs878934420	0.00002
NM_000135.4(FANCA):c.4299C>T (p.Ser1433=)	rs568293451	0.00002
NM_000135.4(FANCA):c.3969C>T (p.Ala1323=)	rs1337959697	0.00001
NM_000135.4(FANCA):c.4251C>T (p.His1417=)	rs752333498	0.00001
NM_000135.4(FANCA):c.3801C>G (p.Gly1267=)	rs143772894
NM_000135.4(FANCA):c.3813A>G (p.Ser1271=)
NM_000135.4(FANCA):c.3850G>C (p.Ala1284Pro)	rs142919010
NM_000135.4(FANCA):c.4335C>T (p.Asp1445=)	rs374830555
NM_001113525.2(ZNF276):c.*1452C>G
NM_001113525.2(ZNF276):c.*1857T>A	rs2151714907
NM_001113525.2(ZNF276):c.*556C>A	rs34602467
NM_001113525.2(ZNF276):c.*604C>G

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