ClinVar Miner

List of variants reported as likely benign for leukoencephalopathy, megalencephalic by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_152722.5(HEPACAM):c.258G>A (p.Glu86=) rs35466065 0.00669
NM_015166.4(MLC1):c.932T>A (p.Val311Glu) rs141225099 0.00622
NM_152722.5(HEPACAM):c.1062C>T (p.Pro354=) rs780208452 0.00017
NM_015166.4(MLC1):c.882G>A (p.Pro294=) rs200163312 0.00001

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