ClinVar Miner

Variants with conflicting interpretations "likely benign" from ClinGen RASopathy Variant Curation Expert Panel and "benign" from any submitter

Minimum review status of the submission from ClinGen RASopathy Variant Curation Expert Panel: Collection method of the submission from ClinGen RASopathy Variant Curation Expert Panel:
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
NM_001354689.3(RAF1):c.581+4A>G rs201776526
NM_002755.4(MAP2K1):c.1098T>C (p.Ala366=) rs200293968
NM_002755.4(MAP2K1):c.69C>T (p.Thr23=) rs140749690
NM_002834.5(PTPN11):c.333-3T>C rs146749153
NM_005633.3(SOS1):c.1705C>G (p.Leu569Val) rs200786705
NM_007373.4(SHOC2):c.1540+8C>T rs771283010
NM_030662.4(MAP2K2):c.1140C>T (p.Ala380=) rs146618055

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