ClinVar Miner

List of variants studied for SLC6A3-related dopamine transporter deficiency syndrome by Neuberg Centre For Genomic Medicine, NCGM

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001044.5(SLC6A3):c.1504G>A (p.Gly502Arg)

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