ClinVar Miner

List of variants reported as likely pathogenic for SLC6A3-related dopamine transporter deficiency syndrome by Invitae

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001044.5(SLC6A3):c.1031+1G>A	rs431905514
NM_001044.5(SLC6A3):c.1156G>A (p.Gly386Arg)
NM_001044.5(SLC6A3):c.1767+2T>C	rs2126324037

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