List of variants in gene PALLD reported as uncertain significance 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_001166108.2(PALLD):c.-83+9G>A	rs150719521	0.00037
NM_001166108.2(PALLD):c.-143A>G	rs571957605	0.00024
NM_001166108.2(PALLD):c.-115C>G	rs189011214	0.00011
NM_001166108.2(PALLD):c.-135A>G	rs540285834	0.00009
NM_001166108.2(PALLD):c.428G>A (p.Arg143His)	rs149345491	0.00006
NM_001166108.2(PALLD):c.1433G>A (p.Gly478Glu)	rs201816881	0.00004
NM_001166108.2(PALLD):c.860G>A (p.Arg287Gln)	rs141283998	0.00002
NM_001166108.2(PALLD):c.-172C>A	rs777479051	0.00001
NM_001166108.2(PALLD):c.-178G>A	rs886059207	0.00001
NM_001166108.2(PALLD):c.107A>G (p.Gln36Arg)	rs889514388	0.00001
NM_001166108.2(PALLD):c.1129A>G (p.Lys377Glu)	rs368684220	0.00001
NM_001166108.2(PALLD):c.1219A>T (p.Thr407Ser)	rs775730191	0.00001
NM_001166108.2(PALLD):c.1260+8T>C	rs887513464	0.00001
NM_001166108.2(PALLD):c.222C>T (p.Ser74=)	rs201038000	0.00001
NM_001166108.2(PALLD):c.836G>C (p.Ser279Thr)	rs886059209	0.00001
NM_001166108.2(PALLD):c.1571G>T (p.Arg524Ile)	rs776908136
NM_001166108.2(PALLD):c.1616C>T (p.Thr539Ile)	rs780510622
NM_001166108.2(PALLD):c.1926C>G (p.Pro642=)	rs886059210
NM_001166108.2(PALLD):c.1957C>A (p.Pro653Thr)	rs1784873065
NM_001166108.2(PALLD):c.574A>G (p.Ser192Gly)	rs1762575507
NM_001166108.2(PALLD):c.622A>G (p.Lys208Glu)
NM_001166108.2(PALLD):c.639C>A (p.Ala213=)	rs1762581096
NM_001166108.2(PALLD):c.721C>T (p.His241Tyr)	rs1490249027
NM_001166108.2(PALLD):c.908+3A>G	rs1762604026
NM_001166108.2(PALLD):c.946G>T (p.Asp316Tyr)	rs1477916241

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