ClinVar Miner

List of variants in gene SLC39A8 reported as uncertain significance for SLC39A8-CDG

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_001135146.2(SLC39A8):c.337T>C (p.Cys113Arg) rs950101299

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