List of variants reported as likely benign for Pancreatic cancer, susceptibility to, 1 by Illumina Laboratory Services, Illumina

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001166108.2(PALLD):c.*317A>T	rs542531106	0.23477
NM_001166108.2(PALLD):c.539C>T (p.Thr180Ile)	rs146387060	0.00071
NM_001166108.2(PALLD):c.2199+8G>A	rs200060953	0.00070
NM_001166108.2(PALLD):c.1842T>A (p.His614Gln)	rs150443035	0.00016
NM_001166108.2(PALLD):c.1386C>T (p.Cys462=)	rs199755853	0.00014
NM_001166108.2(PALLD):c.413G>A (p.Arg138Gln)	rs138665337	0.00007
NM_001166108.2(PALLD):c.229G>C (p.Glu77Gln)	rs376732578	0.00005
NM_001166108.2(PALLD):c.366T>G (p.Pro122=)	rs377747204	0.00005
NM_001166108.2(PALLD):c.2891A>C (p.Asp964Ala)	rs750112132	0.00002
NM_001166108.2(PALLD):c.2867C>T (p.Thr956Ile)	rs371498362	0.00001
NM_001166108.2(PALLD):c.472C>A (p.His158Asn)	rs777197884	0.00001
NM_001166108.2(PALLD):c.608G>T (p.Gly203Val)	rs770458533	0.00001
NM_001166108.2(PALLD):c.1011C>A (p.Asp337Glu)	rs763283965

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