ClinVar Miner

List of variants studied for benign neoplasm by GenomeConnect - Invitae Patient Insights Network

Included ClinVar conditions (133):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_005343.4(HRAS):c.398T>A (p.Leu133His) rs766801436 0.00001
NM_017849.4(TMEM127):c.117_120del (p.Ile41fs) rs121908816

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