List of variants in gene SYN1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_006950.3(SYN1):c.1701A>T (p.Thr567=)	rs770195822	0.00046
NM_006950.3(SYN1):c.1297C>T (p.His433Tyr)	rs41298474	0.00038
NM_006950.3(SYN1):c.1569G>A (p.Ala523=)	rs587781185	0.00022
NM_006950.3(SYN1):c.506G>A (p.Arg169Gln)	rs775109362	0.00007
NM_006950.3(SYN1):c.435+10G>A	rs771547188	0.00004
NM_006950.3(SYN1):c.1971C>T (p.His657=)	rs201236500	0.00002
NM_006950.3(SYN1):c.1008G>A (p.Lys336=)	rs754795220	0.00001
NM_006950.3(SYN1):c.364C>T (p.Pro122Ser)	rs774818779	0.00001
NM_006950.3(SYN1):c.1056-7T>G
NM_006950.3(SYN1):c.213G>C (p.Ser71=)

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