ClinVar Miner

List of variants reported as likely pathogenic for colonic neoplasm by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (19):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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NM_000038.6(APC):c.1312+3A>G rs863225311
NM_000546.5(TP53):c.799C>T (p.Arg267Trp) rs55832599
NM_144997.7(FLCN):c.779+1G>T rs758175953

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