ClinVar Miner

List of variants reported as benign for SLC6A3-related dopamine transporter deficiency syndrome by Genome-Nilou Lab

Included ClinVar conditions (2):

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)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001044.5(SLC6A3):c.1498+14A>G	rs429699	0.97909
NM_001044.5(SLC6A3):c.1031+71G>T	rs40358	0.84277
NM_001044.5(SLC6A3):c.*35T>C	rs1042098	0.31144

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