Infantile Hypotonia-oculomotor Anomalies-hyperkinetic Movements-developmental Delay Syndrome

Other 13 variants 1 gene

Upload your DNA to see your personal risk score for Infantile Hypotonia-oculomotor Anomalies-hyperkinetic Movements-developmental Delay Syndrome.

Associated Genes (1)
Associated Variants (13)
RSID Gene Risk Allele Odds Ratio Evidence
RS1135402761 SYT1 — — strong
RS1565922388 SYT1 — — strong
RS1565922395 SYT1 — — strong
RS1565962725 SYT1 — — strong
RS144900171 SYT1 — — strong
RS1593076474 SYT1 — — strong
RS1882993257 SYT1 — — strong
RS1377017458 SYT1 — — strong
RS2136007608 SYT1 — — strong
RS2136007588 SYT1 — — strong
RS2547785983 SYT1 — — strong
RS2547708515 SYT1 — — strong
RS2547658386 SYT1 — — strong
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