ClinVar Miner

List of variants reported as likely pathogenic by Codex Genetics Limited

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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NM_000021.4(PSEN1):c.781G>A (p.Val261Ile) rs63750964
NM_000166.6(GJB1):c.118G>T (p.Ala40Ser) rs1602348782
NM_007375.3(TARDBP):c.892G>A (p.Gly298Ser) rs4884357
NM_198578.4(LRRK2):c.4883G>C (p.Arg1628Pro) rs33949390

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