List of variants reported as not provided for pancreas disorder by GenomeConnect - Invitae Patient Insights Network

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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_001379610.1(SPINK1):c.101A>G (p.Asn34Ser)	rs17107315	0.00797
NM_003122.5(SPINK1):c.-147A>G	rs779832256	0.00075
NM_024675.4(PALB2):c.3113G>A (p.Trp1038Ter)	rs180177132	0.00002
NM_024675.4(PALB2):c.1616_1617dup (p.Asn540fs)	rs786203346	0.00001
NM_000492.3(CFTR):c.1210-12T[5]	rs1805177
NM_000492.4(CFTR):c.350G>T (p.Arg117Leu)	rs78655421
NM_017774.3(CDKAL1):c.1241del (p.Lys414fs)

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