ClinVar Miner

List of variants reported as likely benign for Behavior disorder

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001045.6(SLC6A4):c.-185C>A rs6354 0.77933
NM_001045.6(SLC6A4):c.*1748C>A rs7224199 0.49153
NM_001045.6(SLC6A4):c.*670T>G rs3813034 0.41083
NM_001045.6(SLC6A4):c.*463T>G rs1042173 0.40123
NM_001045.5(SLC6A4):c.-482T>C rs25533 0.07568
NM_001045.6(SLC6A4):c.*995C>T rs55823902 0.01704
NM_001045.6(SLC6A4):c.*1665T>C rs56138846 0.01363
NM_001045.6(SLC6A4):c.303T>C (p.Asn101=) rs56110451 0.00883
NM_001045.6(SLC6A4):c.-173C>G rs45541837 0.00736
NM_001045.6(SLC6A4):c.1815A>C (p.Lys605Asn) rs6352 0.00450
NM_001045.6(SLC6A4):c.1395C>T (p.Phe465=) rs41274280 0.00237
NM_001045.6(SLC6A4):c.1149C>T (p.Leu383=) rs55908624 0.00196
NM_001045.6(SLC6A4):c.1393T>C (p.Phe465Leu) rs28914833 0.00116
NM_001045.6(SLC6A4):c.*328A>G rs13306796 0.00062
NM_001045.6(SLC6A4):c.*3047A>G rs138050977 0.00053
NM_001045.6(SLC6A4):c.*2703A>G rs189106205 0.00014
NM_001045.6(SLC6A4):c.1368C>T (p.His456=) rs201659393 0.00007
NM_001045.6(SLC6A4):c.*3448G>C rs62068662
NM_001045.6(SLC6A4):c.*597C>T rs185569563

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