ClinVar Miner

List of variants in gene SYN1 reported as benign for X-linked epilepsy-learning disabilities-behavior disorders syndrome

Included ClinVar conditions (1):
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Gene type:
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Total variants: 9
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HGVS dbSNP
NM_006950.3(SYN1):c.1056-14_1056-8del rs377385507
NM_006950.3(SYN1):c.1107C>T (p.Ile369=) rs150248483
NM_006950.3(SYN1):c.1110C>T (p.Cys370=) rs141925310
NM_006950.3(SYN1):c.1297C>T (p.His433Tyr) rs41298474
NM_006950.3(SYN1):c.152C>G (p.Ala51Gly) rs187134574
NM_006950.3(SYN1):c.1699A>G (p.Thr567Ala) rs200533370
NM_006950.3(SYN1):c.426A>G (p.Lys142=) rs145911562
NM_006950.3(SYN1):c.838-8T>G rs12394306
NM_006950.3(SYN1):c.912C>T (p.Ala304=) rs62636605

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