List of variants in gene combination CFTR, LOC111674477 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000492.4(CFTR):c.4333G>A (p.Asp1445Asn)	rs148783445	0.00074
NM_000492.4(CFTR):c.*2G>A	rs150914702	0.00056
NM_000492.4(CFTR):c.4357C>T (p.Arg1453Trp)	rs4148725	0.00009
NM_000492.4(CFTR):c.4340T>A (p.Val1447Glu)	rs1397796355	0.00003
NM_000492.4(CFTR):c.4265G>A (p.Arg1422Gln)	rs780785939	0.00001
NM_000492.4(CFTR):c.4436G>A (p.Arg1479Lys)	rs1325117166	0.00001
NM_000492.4(CFTR):c.4243-16A>G	rs780125251
NM_000492.4(CFTR):c.4243-7del	rs878854021
NM_000492.4(CFTR):c.4324A>G (p.Ser1442Gly)
NM_000492.4(CFTR):c.4423G>T (p.Val1475Leu)	rs369464175

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