ClinVar Miner

List of variants reported as uncertain significance for Macrocephaly, acquired, with impaired intellectual development by New York Genome Center

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_001190737.2(NFIB):c.1217A>G (p.Tyr406Cys) rs750060639 0.00003
NM_001190737.2(NFIB):c.*98G>C rs2118462290
NM_001190738.2(NFIB):c.109-33576G>A rs2132874132

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