ClinVar Miner

List of variants reported as likely benign for amyotrophic lateral sclerosis by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

Included ClinVar conditions (70):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_021076.4(NEFH):c.1740C>T (p.Ser580=) rs114263951 0.00755
NM_007375.4(TARDBP):c.198T>C (p.Ala66=) rs61730366 0.00292

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