ClinVar Miner

List of variants in gene combination CBR4, PALLD reported as uncertain significance for Pancreatic cancer, susceptibility to, 1

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Total variants: 21
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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.*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.*2070G>C rs886059217 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.*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.*1787T>C rs886059215 0.00001
NM_001166108.2(PALLD):c.*2166A>G rs886059220 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.2686C>T (p.Arg896Trp) rs772889018

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