ClinVar Miner

List of variants reported as likely pathogenic for MITF-related melanoma and renal cell carcinoma predisposition syndrome by Integrated Genetics/Laboratory Corporation of America

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_000248.3(MITF):c.952G>A (p.Glu318Lys) rs149617956

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