ClinVar Miner

List of variants in gene KLHL3 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP
NM_017415.2(KLHL3):c.*108G>A rs147305829
NM_017415.2(KLHL3):c.*1106G>T rs141393967
NM_017415.2(KLHL3):c.*1451A>G rs149596381
NM_017415.2(KLHL3):c.*1651C>T rs577834025
NM_017415.2(KLHL3):c.*1896T>G rs75344015
NM_017415.2(KLHL3):c.*2248C>T rs3813317
NM_017415.2(KLHL3):c.*224G>T rs536807069
NM_017415.2(KLHL3):c.*2267T>A rs140696146
NM_017415.2(KLHL3):c.*2360G>A rs533076689
NM_017415.2(KLHL3):c.*2485T>G rs573842978
NM_017415.2(KLHL3):c.*2687C>T rs186283051
NM_017415.2(KLHL3):c.*2805A>G rs141261117
NM_017415.2(KLHL3):c.*299G>A rs539132895
NM_017415.2(KLHL3):c.*3128C>G rs147801381
NM_017415.2(KLHL3):c.*4006C>T rs150624383
NM_017415.2(KLHL3):c.*4065C>T rs142781557
NM_017415.2(KLHL3):c.*4066C>T rs544519958
NM_017415.2(KLHL3):c.-256T>A rs182320171
NM_017415.2(KLHL3):c.-275G>C rs189053795
NM_017415.2(KLHL3):c.-303G>C rs567542768
NM_017415.2(KLHL3):c.1021+5G>A rs183499982
NM_017415.2(KLHL3):c.1321+10C>T rs145091610
NM_017415.2(KLHL3):c.1401C>A (p.Thr467=) rs35420153
NM_017415.2(KLHL3):c.1518C>T (p.Ser506=) rs529937913
NM_017415.2(KLHL3):c.838C>T (p.Leu280=) rs138650966
NM_017415.2(KLHL3):c.904-5C>T rs375172469

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