ClinVar Miner

List of variants reported as uncertain significance for Pancreatic cancer, susceptibility to, 1

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 46
Download table as spreadsheet
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.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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.