List of variants in gene combination FANCA, ZNF276 reported as likely pathogenic by Counsyl

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.4015del (p.Leu1339fs)	rs762902309	0.00004
NM_000135.4(FANCA):c.3913C>T (p.Leu1305Phe)	rs753700179	0.00001
NM_000135.4(FANCA):c.3971C>T (p.Pro1324Leu)	rs182657062	0.00001
NM_000135.4(FANCA):c.4198C>T (p.Arg1400Cys)	rs745882980	0.00001
NM_000135.4(FANCA):c.3884T>A (p.Leu1295Ter)	rs986710868
NM_000135.4(FANCA):c.3884T>G (p.Leu1295Ter)	rs986710868
NM_000135.4(FANCA):c.3890dup (p.Arg1298fs)	rs1555534060
NM_000135.4(FANCA):c.3934+2T>C	rs771775516
NM_000135.4(FANCA):c.3935-1G>T	rs1555533693
NM_000135.4(FANCA):c.4247C>G (p.Ser1416Ter)	rs940187828
NM_000135.4(FANCA):c.4257dup (p.Glu1420fs)	rs1555532946
NM_000135.4(FANCA):c.4260+1G>A	rs1060501887
NM_000135.4(FANCA):c.4260+1dup	rs1555532944
NM_000135.4(FANCA):c.4260+2T>A	rs1555532943

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