ClinVar Miner

List of variants in gene SYN1 reported as benign for developmental disorder of mental health

Included ClinVar conditions (728):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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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