ClinVar Miner

List of variants reported as likely risk allele for Tourette syndrome

Included ClinVar conditions (2):

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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_001407.3(CELSR3):c.2414G>C (p.Ser805Thr)	rs3821875	0.11633
NM_001407.3(CELSR3):c.7853C>T (p.Ala2618Val)	rs138657991	0.00039
NM_001407.3(CELSR3):c.8765G>A (p.Arg2922His)	rs780740673	0.00001

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