ClinVar Miner

List of variants reported as likely benign for adrenal gland disease by Division of Genomic Diagnostics,The Children's Hospital of Philadelphia

Included ClinVar conditions (124):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_000551.3(VHL):c.271T>G (p.Phe91Val) rs1559426039
NM_000551.3(VHL):c.340+7G>C rs869025635
NM_000551.3(VHL):c.340+8C>T rs756068442
NM_000551.3(VHL):c.341-21_341-17delAACCT rs869025639
NM_000551.3(VHL):c.463+37_463+39del rs869025658
NM_000551.3(VHL):c.463+8C>T rs5030834
NM_000551.3(VHL):c.598C>T (p.Arg200Trp) rs28940298

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