ClinVar Miner

List of variants in gene combination FANCA, ZNF276 reported as benign for DNA repair disease

Included ClinVar conditions (124):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001113525.2(ZNF276):c.*1693A>T rs7195906 0.53795
NM_001113525.2(ZNF276):c.1574+23del rs17233826 0.48664
NM_001113525.2(ZNF276):c.*1323G>A rs1061646 0.40513
NM_000135.4(FANCA):c.3807G>C (p.Leu1269=) rs11649210 0.11105
NM_000135.4(FANCA):c.3982A>G (p.Thr1328Ala) rs9282681 0.05868
NM_001113525.2(ZNF276):c.1475-191C>T rs16966023 0.04351
NM_001113525.2(ZNF276):c.1574+23T>C rs62704561 0.03426
NM_001113525.2(ZNF276):c.*103C>G rs17233797 0.03296
NM_001113525.2(ZNF276):c.1815G>C (p.Glu605Asp) rs17227424 0.02929
NM_000135.4(FANCA):c.3859G>A (p.Val1287Ile) rs17227354 0.02526
NM_001113525.2(ZNF276):c.*68C>T rs17227417 0.02259
NM_001113525.2(ZNF276):c.1574+26C>A rs17233812 0.01850
NM_001113525.2(ZNF276):c.1475-216G>A rs17227452 0.01670
NM_001113525.2(ZNF276):c.1574+17A>C rs17233833 0.01627
NM_001113525.2(ZNF276):c.*1316C>T rs9282680 0.01028
NM_000135.4(FANCA):c.4249C>G (p.His1417Asp) rs17227403 0.00362
NM_000135.4(FANCA):c.3891G>A (p.Lys1297=) rs17227361 0.00286
NM_000135.4(FANCA):c.4332T>G (p.Pro1444=) rs149531696 0.00072
NM_000135.4(FANCA):c.4036G>A (p.Ala1346Thr) rs17227396 0.00056
NM_001113525.2(ZNF276):c.*69G>A rs17233804 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.4177G>A (p.Val1393Met) rs199652831 0.00009
NM_000135.4(FANCA):c.4226G>A (p.Arg1409Gln) rs370507983 0.00006
NM_000135.4(FANCA):c.4244T>G (p.Phe1415Cys) rs201658945 0.00006
NM_001113525.2(ZNF276):c.*201C>T rs1230
NM_001113525.2(ZNF276):c.*523_*538del
NM_001113525.2(ZNF276):c.*607A>G rs1800359

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