ClinVar Miner

List of variants in gene PEX13 reported as uncertain significance 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: 45
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HGVS dbSNP
NM_002618.4(PEX13):c.*1283C>G rs886056201
NM_002618.4(PEX13):c.*1377G>A rs536283006
NM_002618.4(PEX13):c.*1533G>C rs886056202
NM_002618.4(PEX13):c.*1564C>G rs886056203
NM_002618.4(PEX13):c.*1566A>T rs886056204
NM_002618.4(PEX13):c.*1724A>T rs137932203
NM_002618.4(PEX13):c.*1875_*1876del rs886056205
NM_002618.4(PEX13):c.*1961T>C rs771587917
NM_002618.4(PEX13):c.*1998T>C rs559684247
NM_002618.4(PEX13):c.*2159T>C rs886056206
NM_002618.4(PEX13):c.*2168A>T rs886056207
NM_002618.4(PEX13):c.*216T>C rs146980377
NM_002618.4(PEX13):c.*2296G>A rs886056208
NM_002618.4(PEX13):c.*233G>T rs886056198
NM_002618.4(PEX13):c.*2356T>C rs139999174
NM_002618.4(PEX13):c.*263A>T rs558525565
NM_002618.4(PEX13):c.*2642T>C rs886056209
NM_002618.4(PEX13):c.*2989_*2990del rs886056210
NM_002618.4(PEX13):c.*298G>C rs886056199
NM_002618.4(PEX13):c.*3012A>G rs144691386
NM_002618.4(PEX13):c.*3038A>T rs886056211
NM_002618.4(PEX13):c.*3044del rs886056212
NM_002618.4(PEX13):c.*383A>T rs149099359
NM_002618.4(PEX13):c.*442dup rs201619544
NM_002618.4(PEX13):c.*676A>G rs886056200
NM_002618.4(PEX13):c.*803A>G rs561112537
NM_002618.4(PEX13):c.*813G>C rs781689721
NM_002618.4(PEX13):c.*90A>G rs535967834
NM_002618.4(PEX13):c.*944C>T rs148184159
NM_002618.4(PEX13):c.*956G>T rs141215166
NM_002618.4(PEX13):c.1078C>G (p.Leu360Val) rs74350038
NM_002618.4(PEX13):c.1158G>A (p.Lys386=) rs371789976
NM_002618.4(PEX13):c.1180A>T (p.Ile394Phe)
NM_002618.4(PEX13):c.193A>G (p.Ser65Gly) rs886056196
NM_002618.4(PEX13):c.260A>G (p.Asn87Ser) rs367843599
NM_002618.4(PEX13):c.269A>G (p.Tyr90Cys) rs200928725
NM_002618.4(PEX13):c.275G>A (p.Gly92Asp) rs745620818
NM_002618.4(PEX13):c.338T>C (p.Leu113Pro) rs202077756
NM_002618.4(PEX13):c.355G>A (p.Val119Ile) rs147707348
NM_002618.4(PEX13):c.383G>T (p.Gly128Val) rs554152771
NM_002618.4(PEX13):c.417A>G (p.Ala139=) rs886056197
NM_002618.4(PEX13):c.464A>G (p.Tyr155Cys) rs1298522041
NM_002618.4(PEX13):c.478G>C (p.Ala160Pro) rs1559035602
NM_002618.4(PEX13):c.791G>C (p.Ser264Thr) rs145568490
NM_002618.4(PEX13):c.856G>A (p.Val286Ile) rs201699810

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