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

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001113525.2(ZNF276):c.*841G>A	rs191404781	0.00092
NM_000135.4(FANCA):c.3971C>T (p.Pro1324Leu)	rs182657062	0.00001
NM_000135.4(FANCA):c.4069_4082del (p.Ala1357fs)	rs747892390	0.00001
NM_000135.4(FANCA):c.3782TCT[2] (p.Phe1263del)	rs397507553
NM_000135.4(FANCA):c.4010+1_4010+18del	rs752457319
NM_000135.4(FANCA):c.4011-1G>A	rs761988162
NM_000135.4(FANCA):c.4021_4027del (p.Tyr1341fs)	rs2151712033
NM_000135.4(FANCA):c.4096C>T (p.Gln1366Ter)	rs1336834251
NM_000135.4(FANCA):c.4124_4125del (p.Thr1375fs)	rs776969626

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