ClinVar Miner

List of variants in gene PEX10, RER1 studied for Zellweger spectrum disorders

Included ClinVar conditions (47):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_002617.4(PEX10):c.*686C>G rs41310349 0.00448
NM_002617.4(PEX10):c.*676C>T rs77863194 0.00408
NM_002617.4(PEX10):c.*595G>A rs72924937 0.00377
NM_002617.4(PEX10):c.*643C>T rs150136015 0.00177
NM_002617.4(PEX10):c.*410G>A rs886046144 0.00099
NM_002617.4(PEX10):c.*854G>A rs556816263 0.00053
NM_002617.4(PEX10):c.*420G>A rs868844283 0.00025
NM_002617.4(PEX10):c.*401A>C rs866387988 0.00023
NM_002617.4(PEX10):c.*835C>T rs886046136 0.00010
NM_002617.4(PEX10):c.*732G>A rs886046140 0.00007
NM_002617.4(PEX10):c.*594C>T rs760677467 0.00006
NM_002617.4(PEX10):c.*627C>T rs886046142 0.00006
NM_002617.4(PEX10):c.*499G>A rs886046143 0.00004
NM_002617.4(PEX10):c.*905A>C rs1316891759 0.00002
NM_002617.4(PEX10):c.*445G>A rs557941413 0.00001
NM_002617.4(PEX10):c.*824G>A rs1288938989 0.00001
NM_002617.4(PEX10):c.*838C>T rs886046135 0.00001
NM_002617.4(PEX10):c.*352G>A rs115735911
NM_002617.4(PEX10):c.*688G>T rs886046141
NM_002617.4(PEX10):c.*744dup rs886046139
NM_002617.4(PEX10):c.*782C>A rs886046138
NM_002617.4(PEX10):c.*798C>T rs886046137
NM_002617.4(PEX10):c.*951G>C rs1642943783

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