List of variants in gene PALLD reported as likely benign for Pancreatic cancer, susceptibility to, 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001166108.2(PALLD):c.502C>G (p.Leu168Val)	rs115607645	0.00299
NM_001166108.2(PALLD):c.764G>A (p.Arg255His)	rs146018183	0.00287
NM_001166108.2(PALLD):c.1965-12594T>G	rs587780760	0.00102
NM_001166108.2(PALLD):c.539C>T (p.Thr180Ile)	rs146387060	0.00071
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.-8G>A	rs372273201	0.00006
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.1965-12800C>T	rs863224383	0.00002
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
NM_001166108.2(PALLD):c.296C>A (p.Ser99Ter)
NM_001166108.2(PALLD):c.353C>G (p.Ser118Ter)

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