ClinVar Miner

Variants with conflicting interpretations "likely benign" from CeGaT Center for Human Genetics Tuebingen and "drug response" from any submitter

Minimum review status of the submission from CeGaT Center for Human Genetics Tuebingen: Collection method of the submission from CeGaT Center for Human Genetics Tuebingen:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 7
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HGVS dbSNP gnomAD frequency
NM_000041.2(APOE):c.526C>T (p.Arg176Cys) rs7412 0.07986
NM_000110.4(DPYD):c.1236G>A (p.Glu412=) rs56038477 0.01297
NM_000914.5(OPRM1):c.575G>T (p.Cys192Phe) rs62638690 0.00573
NM_000914.5(OPRM1):c.-25C>T rs41292890 0.00226
NM_024006.6(VKORC1):c.106G>T (p.Asp36Tyr) rs61742245 0.00150
NM_003977.4(AIP):c.911G>A (p.Arg304Gln) rs104894190 0.00115
NM_024426.6(WT1):c.411G>C (p.Pro137=) rs1332588174

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