List of variants in gene SYN1 reported as benign for epilepsy, X-linked 1, with variable learning disabilities and behavior disorders

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_006950.3(SYN1):c.510T>C (p.Asn170=)	rs1142636	0.39391
NM_006950.3(SYN1):c.1699A>G (p.Thr567Ala)	rs200533370	0.01462
NM_006950.3(SYN1):c.912C>T (p.Ala304=)	rs62636605	0.01433
NM_006950.3(SYN1):c.152C>G (p.Ala51Gly)	rs187134574	0.01317
NM_006950.3(SYN1):c.838-8T>G	rs12394306	0.01234
NM_006950.3(SYN1):c.528-19C>T	rs190935498	0.00192
NM_006950.3(SYN1):c.980+14C>T	rs376734047	0.00157
NM_006950.3(SYN1):c.1107C>T (p.Ile369=)	rs150248483	0.00107
NM_006950.3(SYN1):c.1110C>T (p.Cys370=)	rs141925310	0.00101
NM_006950.3(SYN1):c.426A>G (p.Lys142=)	rs145911562	0.00054
NM_006950.3(SYN1):c.1297C>T (p.His433Tyr)	rs41298474	0.00038
NM_006950.3(SYN1):c.1055+12G>A	rs373071109	0.00021
NM_006950.3(SYN1):c.999G>T (p.Gly333=)	rs752926074	0.00019
NM_006950.3(SYN1):c.980+20C>A	rs777705880	0.00014
NM_006950.3(SYN1):c.981-19C>T	rs375349005	0.00007
NM_006950.3(SYN1):c.1056-14_1056-8del	rs377385507
NM_006950.3(SYN1):c.144C>G (p.Thr48=)
NM_006950.3(SYN1):c.1821G>T (p.Ala607=)

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