ClinVar Miner

List of variants reported as uncertain significance for adrenal gland neoplasm by Institute of Human Genetics, University of Leipzig Medical Center

Included ClinVar conditions (49):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_001370259.2(MEN1):c.803A>G (p.Tyr268Cys) rs773500082 0.00006
NM_017841.4(SDHAF2):c.352A>G (p.Ile118Val) rs747994812 0.00001
NM_001370259.2(MEN1):c.1003C>T (p.Arg335Trp) rs371364206
NM_001370259.2(MEN1):c.1185+1G>A rs1941661315
NM_001370259.2(MEN1):c.1780A>G (p.Thr594Ala) rs1941488490

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