ClinVar Miner

List of variants studied for demyelinating hereditary motor and sensory neuropathy by Equipe Genetique des Anomalies du Developpement,Université de Bourgogne

Included ClinVar conditions (46):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP
NM_024577.3(SH3TC2):c.2431C>T
NM_024577.3(SH3TC2):c.3676-8G>A rs772823083

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