ClinVar Miner

List of variants in gene SLC9A6 reported as uncertain significance for Astigmatism; Leukodystrophy; Motor delay; Seizure; Short stature; Hypermetropia; Delayed speech and language development; Open mouth; Microcephaly; Strabismus; Amblyopia; EEG with generalized slow activity; Allergy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001379110.1(SLC9A6):c.1190C>A (p.Ala397Glu) rs1556619324

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