ClinVar Miner

Variants with conflicting interpretations "benign" from H3Africa Consortium and "likely benign" from any submitter

Minimum review status of the submission from H3Africa Consortium: Collection method of the submission from H3Africa Consortium:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 6
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HGVS dbSNP gnomAD frequency
NM_001308093.3(GATA4):c.617-113T>C rs3735819 0.80128
NM_002843.4(PTPRJ):c.827A>C (p.Gln276Pro) rs1566734 0.14574
NM_001174096.2(ZEB1):c.233A>C (p.Asn78Thr) rs80194531 0.01629
NM_000483.5(APOC2):c.229A>C (p.Lys77Gln) rs5126 0.00784
NM_000041.4(APOE):c.487C>T (p.Arg163Cys) rs769455 0.00701
NM_002875.5(RAD51):c.449G>A (p.Arg150Gln) rs121917739 0.00171

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