ClinVar Miner

List of variants in gene GMNN reported as pathogenic for Meier-Gorlin syndrome 6

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_015895.5(GMNN):c.16A>T (p.Lys6Ter) rs864309486
NM_015895.5(GMNN):c.35_38del (p.Ile12fs) rs864309487
NM_015895.5(GMNN):c.50A>G (p.Lys17Arg) rs864309488

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