ClinVar Miner

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

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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_001166108.2(PALLD):c.*2141A>G rs962914167 0.00071
NM_001166108.2(PALLD):c.*1792T>A rs186567215 0.00070
NM_001166108.2(PALLD):c.*2027T>C rs192990293 0.00065
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.*1131T>G rs773353973 0.00023
NM_001166108.2(PALLD):c.*2184G>A rs769635594 0.00020
NM_001166108.2(PALLD):c.*2171T>C rs548951283 0.00014
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.*2070G>C rs886059217 0.00006
NM_001166108.2(PALLD):c.428G>A (p.Arg143His) rs149345491 0.00006
NM_001166108.2(PALLD):c.*439T>C rs972893704 0.00005
NM_001166108.2(PALLD):c.*2022A>G rs886059216 0.00004
NM_001166108.2(PALLD):c.1433G>A (p.Gly478Glu) rs201816881 0.00004
NM_001166108.2(PALLD):c.*1655A>T rs976050795 0.00003
NM_001166108.2(PALLD):c.*1808C>T rs539762995 0.00003
NM_001166108.2(PALLD):c.*908A>G rs886059212 0.00003
NM_001166108.2(PALLD):c.*400T>C rs748402946 0.00002
NM_001166108.2(PALLD):c.860G>A (p.Arg287Gln) rs141283998 0.00002
NM_001166108.2(PALLD):c.*1787T>C rs886059215 0.00001
NM_001166108.2(PALLD):c.*2166A>G rs886059220 0.00001
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.*1713T>C rs765552955
NM_001166108.2(PALLD):c.*1757T>G rs886059214
NM_001166108.2(PALLD):c.*2168C>A rs886059221
NM_001166108.2(PALLD):c.*386T>C rs575876255
NM_001166108.2(PALLD):c.*461G>A rs939786378
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.2686C>T (p.Arg896Trp) rs772889018
NM_001166108.2(PALLD):c.574A>G (p.Ser192Gly) rs1762575507
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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