List of variants reported as not provided for pancreas disorder by GenomeConnect, ClinGen

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000492.4(CFTR):c.1584G>A (p.Glu528=)	rs1800095	0.01670
NM_001379610.1(SPINK1):c.101A>G (p.Asn34Ser)	rs17107315	0.00797
NM_000525.4(KCNJ11):c.47G>A (p.Arg16His)	rs770609243	0.00003
GRCh37/hg19 17q21.31(chr17:41230488-41235856)x3
NM_000059.4(BRCA2):c.8817_8820del (p.Lys2939fs)	rs397508010
NM_000162.5(GCK):c.1085C>T (p.Thr362Ile)	rs2096271812

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