ClinVar Miner

List of variants reported as likely pathogenic for cardiovascular organ benign neoplasm by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_000546.5(TP53):c.799C>T (p.Arg267Trp) rs55832599
NM_000551.3(VHL):c.319C>G (p.Arg107Gly) rs397516440
NM_020975.6(RET):c.1947G>A (p.Ser649=) rs377767412

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