List of variants in gene CFTR, LOC111674472 studied for Hereditary pancreatitis

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000492.4(CFTR):c.3285A>T (p.Thr1095=)	rs1800118	0.00570
NM_000492.4(CFTR):c.3154T>G (p.Phe1052Val)	rs150212784	0.00039
NM_000492.4(CFTR):c.3205G>A (p.Gly1069Arg)	rs200321110	0.00035
NM_000492.4(CFTR):c.3209G>A (p.Arg1070Gln)	rs78769542	0.00006
NM_000492.4(CFTR):c.3033A>G (p.Leu1011=)	rs773752573	0.00002
NM_000492.4(CFTR):c.3118C>T (p.Leu1040Phe)	rs1562914212
NM_000492.4(CFTR):c.3301del (p.Gln1100_Met1101insTer)	rs2116085156

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