ClinVar Miner

List of variants reported as uncertain significance for benign neoplasm by New York Genome Center

Included ClinVar conditions (123):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_017617.5(NOTCH1):c.5674G>A (p.Gly1892Arg) rs761427888 0.00001
NM_015922.3(NSDHL):c.1054C>G (p.Leu352Val) rs142351862

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