Severe Myoclonic Epilepsy in Infancy

Neurological 604 variants 1 gene

Upload your DNA to see your personal risk score for Severe Myoclonic Epilepsy in Infancy.

Associated Genes (1)

SCN1A

Associated Variants (604)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS121917945	SCN1A	—	—	strong
RS121917965	SCN1A	—	—	strong
RS121917918	SCN1A	—	—	strong
RS121917963	SCN1A	—	—	strong
RS121917911	SCN1A	—	—	strong
RS121917973	SCN1A	—	—	strong
RS121917912	SCN1A	—	—	strong
RS121917910	SCN1A	—	—	strong
RS121917960	SCN1A	—	—	strong
RS121917986	SCN1A	—	—	strong
RS121917987	SCN1A	—	—	strong
RS121917913	SCN1A	—	—	strong
RS121917974	SCN1A	—	—	strong
RS121917972	SCN1A	—	—	strong
RS121917992	SCN1A	—	—	strong
RS121917975	SCN1A	—	—	strong
RS121917919	SCN1A	—	—	strong
RS121917993	SCN1A	—	—	strong
RS121917915	SCN1A	—	—	strong
RS121917914	SCN1A	—	—	strong
RS121917995	SCN1A	—	—	strong
RS121917976	SCN1A	—	—	strong
RS121917949	SCN1A	—	—	strong
RS121917926	SCN1A	—	—	strong
RS777631884	SCN1A	—	—	strong
RS397514458	SCN1A	—	—	strong
RS121918623	SCN1A	—	—	strong
RS121917954	SCN1A	—	—	strong
RS121917955	SCN1A	—	—	strong
RS1574272192	SCN1A	—	—	strong
RS121918624	SCN1A	—	—	strong
RS121918625	SCN1A	—	—	strong
RS121918628	SCN1A	—	—	strong
RS121918629	SCN1A	—	—	strong
RS121918630	SCN1A	—	—	strong
RS121918631	SCN1A	—	—	strong
RS1574061044	SCN1A	—	—	strong
RS121918632	SCN1A	—	—	strong
RS121918622	SCN1A	—	—	strong
RS397514459	SCN1A	—	—	strong
RS121917923	SCN1A	—	—	strong
RS121917957	SCN1A	—	—	strong
RS121917929	SCN1A	—	—	strong
RS121917927	SCN1A	—	—	strong
RS121917966	SCN1A	—	—	strong
RS121917967	SCN1A	—	—	strong
RS121917990	SCN1A	—	—	strong
RS121917941	SCN1A	—	—	strong
RS121917964	SCN1A	—	—	strong
RS121917971	SCN1A	—	—	strong

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