ClinVar Miner

List of variants in gene SETBP1 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_015559.3(SETBP1):c.*1160del rs566863613
NM_015559.3(SETBP1):c.*1163G>A rs368967558
NM_015559.3(SETBP1):c.*1533T>C rs192597791
NM_015559.3(SETBP1):c.*1817A>G rs9963575
NM_015559.3(SETBP1):c.*2259A>T rs1349385
NM_015559.3(SETBP1):c.*2405T>C rs149990348
NM_015559.3(SETBP1):c.*2414C>G rs373681388
NM_015559.3(SETBP1):c.*2688A>G rs568234066
NM_015559.3(SETBP1):c.*2791A>G rs142310022
NM_015559.3(SETBP1):c.*2884C>T rs112813646
NM_015559.3(SETBP1):c.*3179G>A rs72898811
NM_015559.3(SETBP1):c.*3288C>G rs146961449
NM_015559.3(SETBP1):c.*3313A>C rs557394901
NM_015559.3(SETBP1):c.*3434T>C rs148016914
NM_015559.3(SETBP1):c.*3573G>A rs566520020
NM_015559.3(SETBP1):c.*3676C>T rs117464906
NM_015559.3(SETBP1):c.*3829C>T rs141617886
NM_015559.3(SETBP1):c.*3833C>G rs181283064
NM_015559.3(SETBP1):c.*3839A>T rs560511856
NM_015559.3(SETBP1):c.*3884T>G rs117797575
NM_015559.3(SETBP1):c.*4010C>T rs150522461
NM_015559.3(SETBP1):c.*4237C>A rs143072709
NM_015559.3(SETBP1):c.*4240T>C rs569151004
NM_015559.3(SETBP1):c.*4259A>T rs567262571
NM_015559.3(SETBP1):c.*4266dup rs536376470
NM_015559.3(SETBP1):c.*4510T>C rs76077260
NM_015559.3(SETBP1):c.-164C>G rs145284354
NM_015559.3(SETBP1):c.-248G>T rs563748893
NM_015559.3(SETBP1):c.1037C>T (p.Thr346Ile) rs557430935
NM_015559.3(SETBP1):c.1158C>T (p.Asn386=) rs73472918
NM_015559.3(SETBP1):c.1170C>T (p.Ala390=) rs8091231
NM_015559.3(SETBP1):c.141G>A (p.Gly47=) rs146868426
NM_015559.3(SETBP1):c.1483T>A (p.Ser495Thr) rs138515058
NM_015559.3(SETBP1):c.1490C>T (p.Pro497Leu) rs145133915
NM_015559.3(SETBP1):c.1491G>A (p.Pro497=) rs113053616
NM_015559.3(SETBP1):c.1581T>G (p.Ala527=) rs150136756
NM_015559.3(SETBP1):c.1828G>A (p.Val610Ile) rs200927313
NM_015559.3(SETBP1):c.1932C>T (p.Ser644=) rs3744824
NM_015559.3(SETBP1):c.2310G>A (p.Ala770=) rs373845529
NM_015559.3(SETBP1):c.2607C>T (p.Ser869=) rs74499808
NM_015559.3(SETBP1):c.2873A>G (p.Glu958Gly) rs748289164
NM_015559.3(SETBP1):c.3237T>C (p.Leu1079=) rs150875847
NM_015559.3(SETBP1):c.3299A>G (p.His1100Arg) rs149162154
NM_015559.3(SETBP1):c.3576C>T (p.Ser1192=) rs201826395
NM_015559.3(SETBP1):c.3618T>C (p.His1206=) rs34882016
NM_015559.3(SETBP1):c.3681G>A (p.Glu1227=) rs377760121
NM_015559.3(SETBP1):c.3883G>A (p.Val1295Met) rs563768215
NM_015559.3(SETBP1):c.4073T>C (p.Met1358Thr) rs569465675
NM_015559.3(SETBP1):c.4096G>A (p.Ala1366Thr) rs145549368
NM_015559.3(SETBP1):c.4129G>C (p.Val1377Leu) rs77518617
NM_015559.3(SETBP1):c.4209G>A (p.Glu1403=) rs565949588
NM_015559.3(SETBP1):c.4234C>A (p.Arg1412=) rs145996171
NM_015559.3(SETBP1):c.4398G>T (p.Glu1466Asp) rs117498128
NM_015559.3(SETBP1):c.4554G>A (p.Glu1518=) rs574196735
NM_015559.3(SETBP1):c.685G>A (p.Gly229Arg) rs143196787
NM_015559.3(SETBP1):c.85G>A (p.Ala29Thr) rs772172102

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