List of variants in gene combination FANCA, ZNF276 reported as likely 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.4015del (p.Leu1339fs)	rs762902309	0.00004
NM_000135.4(FANCA):c.4199G>A (p.Arg1400His)	rs149851163	0.00003
NM_000135.4(FANCA):c.3791_3793del (p.Ser1264del)	rs1183256870
NM_000135.4(FANCA):c.3934+1G>C
NM_000135.4(FANCA):c.4010+1_4010+18del	rs752457319
NM_000135.4(FANCA):c.4010+2T>C	rs2062067746
NM_000135.4(FANCA):c.4124_4125del (p.Thr1375fs)	rs776969626

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