ClinVar Miner

List of variants in gene combination BANF1, EIF1AD, LOC130006089 reported as likely benign for Nestor-Guillermo progeria syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001242481.2(EIF1AD):c.-329G>A rs117774800 0.00044

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